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Healthcare Essential Electrical Systems

Written and maintained by SynC.

Rev4
IssuedOct 19, 2026
LicenseCC BY 4.0
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1 Scope

NOTE This standard governs the essential electrical system of a health care facility as one system: the risk categories that decide what the facility needs, the type of system those categories require, the branches the system is divided into and the loads each branch carries, the performance the alternate source owes the branches, the transfer switches that serve them, the wiring that keeps them independent, the circuits and receptacles at the patient bed, the ground-fault protection and the isolated power that protect the patient, the coordination requirement that applies to the whole system, and the tests and records that prove the system and keep it provable through its life. (1.1)
NOTE The essential electrical system is a layer over the emergency and standby power system, not a replacement for it: NFPA 70 Article 517 applies Article 700 to the life safety branch and amends it, and NFPA 99 adds the risk categories, the branch structure, the equipment branch sequence, and a testing regime of its own. The system-level decisions that are not specific to health care, including the alternate source redundancy, the transfer type, the neutral treatment, and the integrated acceptance test, are made under Emergency And Standby PowerEmergency and Standby Power SystemsResolves to the current adopted revision.sync/emergency-and-standby-power and are not repeated here. (1.2)
NOTE The following are governed elsewhere and are outside this standard: (1.3)
  • the alternate source redundancy, the transfer type and neutral treatment across the system, and the integrated acceptance test under NFPA 110 Chapter 7 (Emergency And Standby PowerEmergency and Standby Power SystemsResolves to the current adopted revision.sync/emergency-and-standby-power)
  • the engine-generator set, its fuel system on the skid, its controller, and its remote annunciator (GeneratorsEngine GeneratorsResolves to the current adopted revision.sync/generators)
  • the assembly that synchronizes multiple machines onto one bus and its load add and load shed tables (Generator Paralleling SwitchgearGenerator Paralleling SwitchgearResolves to the current adopted revision.sync/generator-paralleling-switchgear)
  • the switch itself, with its mechanism, its ratings, its time delays, and its enclosure (Automatic Transfer SwitchesAutomatic Transfer SwitchesResolves to the current adopted revision.sync/automatic-transfer-switches)
  • the panelboard as a product (PanelboardsPanelboardsResolves to the current adopted revision.sync/panelboards) and the raceway products and their installation (Raceways And ConduitRaceways and ConduitResolves to the current adopted revision.sync/raceways-and-conduit)
  • the device as a product, with its grade, its configuration, and its color (Wiring DevicesWiring DevicesResolves to the current adopted revision.sync/wiring-devices)
  • the redundant grounding of each patient care space and the grounding test NFPA 99 requires there (Grounding And BondingGrounding and Bonding for Electrical SystemsResolves to the current adopted revision.sync/grounding-and-bonding)
  • the short-circuit study that establishes the available fault current at the system (Short Circuit StudyShort-Circuit StudyResolves to the current adopted revision.sync/short-circuit-study) and the coordination study itself and the settings it recommends (Protective Coordination StudyProtective Device Coordination StudyResolves to the current adopted revision.sync/protective-coordination-study)
  • the egress lighting itself (Emergency And Egress LightingEmergency and Egress LightingResolves to the current adopted revision.sync/emergency-and-egress-lighting)
  • the fire alarm system (Fire Alarm SystemsFire Alarm SystemsResolves to the current adopted revision.sync/fire-alarm-systems), the nurse call system (Nurse Call SystemsNurse Call SystemsResolves to the current adopted revision.sync/nurse-call-systems), and the medical gas source equipment and alarms (Medical Gas SystemsMedical Gas and Vacuum SystemsResolves to the current adopted revision.sync/medical-gas-systems) that this system supplies
1.4 The Contractor shall coordinate the branch assignment of every load, the transfer switch arrangement, the alternate source performance, and the ground-fault protection scheme with the standards named in this section before any transfer switch, distribution equipment, or isolated power panel is released for manufacture.

2 Referenced Standards

2.1 Design, equipment, and installation shall comply with the latest edition of each of the following that the Authority Having Jurisdiction has adopted, unless a specific edition is cited.
2.2 Where the adopted editions of NFPA 70 and NFPA 99 differ on a requirement of the essential electrical system, the more stringent requirement shall govern unless the Authority Having Jurisdiction accepts the less stringent one in writing.
NOTE The Centers for Medicare and Medicaid Services adopt NFPA 99 and NFPA 101 by edition in the Conditions of Participation, and the edition they adopt is routinely older than the one the state has adopted, so a facility that bills Medicare answers to two editions at once; the more stringent of the two is the one a surveyor can cite. (2.3)
Standard Title
NFPA 70 National Electrical Code (Article 517, with Articles 700 and 701 as Article 517 applies them)
NFPA 99 Health Care Facilities Code
NFPA 110 Standard for Emergency and Standby Power Systems
NFPA 101 Life Safety Code
UL 1008 Transfer Switch Equipment
UL 1047 Isolated Power Systems Equipment
UL 1022 Line Isolation Monitors
UL 2200 Stationary Engine Generator Assemblies
IEEE 602 Recommended Practice for Electric Systems in Health Care Facilities
ANSI/ASHRAE/ASHE 170 Ventilation of Health Care Facilities
FGI Guidelines Guidelines for Design and Construction of Hospitals
ASCE/SEI 7 Minimum Design Loads and Associated Criteria for Buildings and Other Structures
ANSI/NETA ATS Standard for Acceptance Testing Specifications for Electrical Power Equipment and Systems
42 CFR Part 482 Conditions of Participation for Hospitals
42 CFR Part 483 Requirements for Long Term Care Facilities

3 Submittals

3.1 Action Submittals

3.1.1 The Contractor shall submit the following for review before any transfer switch, branch distribution equipment, or isolated power panel is released for manufacture:
  • a one-line diagram of the complete essential electrical system showing the normal source, each alternate source, every transfer switch with the branch it serves, every branch panelboard and distribution board, and the feeders between them
  • a branch load schedule assigning every load the system serves to the life safety, critical, or equipment branch, citing the NFPA 70 517.32, 517.33, or 517.34 provision that places it there, and stating for each equipment branch load whether it is connected automatically, by delayed automatic connection, or manually
  • a classification statement giving the risk category of each patient care space the system serves as the governing body determined it, the essential electrical system type that follows, and the NFPA 110 level, type, and class of the alternate source
  • the demand calculation for the essential electrical system on the basis the datasheet selects, carried to each transfer switch and each branch
  • a transfer switch schedule giving, for each switch, the branch served, the bypass-isolation selection, and the connection delay, consistent with the product data submitted under Automatic Transfer SwitchesAutomatic Transfer SwitchesResolves to the current adopted revision.sync/automatic-transfer-switches
  • the wiring plan for the life safety and critical branches, showing the wiring method of each feeder and branch circuit and every point where the branch wiring enters an enclosure that another system also enters
  • the ground-fault protection arrangement, showing each level of protection, the device that provides it, and the pickup and time delay the coordination study assigns to it
  • product data for each isolated power panel, its line isolation monitor, its remote indicator, and its receptacles, with the UL 1047 and UL 1022 listings
  • the receptacle identification schedule for the life safety and critical branches, consistent with the device color schedule submitted under Wiring DevicesWiring DevicesResolves to the current adopted revision.sync/wiring-devices
Action Submittalscheckbox
☑ Essential electrical system one-line diagram
☑ Branch load schedule with the code basis of each assignment
☑ Classification statement of risk categories, system type, and NFPA 110 level, type, and class
☑ Essential electrical system demand calculation
☑ Transfer switch schedule with branch, bypass-isolation, and delay
☑ Life safety and critical branch wiring plan
☑ Ground-fault protection arrangement with study settings
☐ Isolated power system product data
☐ Receptacle identification schedule
3.1.2 No transfer switch, branch distribution equipment, or isolated power panel shall be released for manufacture until the one-line diagram, the branch load schedule, and the classification statement have been reviewed and returned.
NOTE The branch load schedule is the submittal that decides whether the system passes its first survey, because a load on the wrong branch is a finding regardless of how well the equipment performs, and the schedule is the only document in which every load and its branch appear side by side with the provision that put it there. (3.1.3)

3.2 Informational Submittals

3.2.1 The Contractor shall submit the following with or before the action submittals:
  • a copy of the governing body's risk assessment under NFPA 99 Chapter 4 for the spaces the system serves, or the written statement of the categories it assigned
  • the portion of the coordination study prepared under Protective Coordination StudyProtective Device Coordination StudyResolves to the current adopted revision.sync/protective-coordination-study that demonstrates the coordination NFPA 70 517.31(G) requires for the essential electrical system
  • a restoration time budget showing the time from loss of the normal source to energization of the life safety and critical branches, with the engine start, the source acceptance, and each transfer switch delay itemized
  • the qualification statement of the firm that will test the isolated power systems and the patient care receptacles
  • the acceptance test procedure for the essential electrical system, covering every test this standard requires
Informational Submittalscheckbox
☑ Governing body's risk assessment or category statement
☑ Coordination study extract for NFPA 70 517.31(G)
☑ Restoration time budget
☐ Isolated power and receptacle testing firm qualification
☑ Acceptance test procedure

3.3 Closeout Submittals

3.3.1 The Contractor shall submit the following before the essential electrical system is accepted:
  • the as-built one-line diagram and branch load schedule reflecting every field change and the branch assignment as installed
  • the acceptance test records for the system, giving the measured restoration time of each branch, the equipment branch connection sequence and delays as commissioned, the ground-fault protection performance test record NFPA 70 517.17(D) requires, every isolated power system and line isolation monitor test, and every patient care receptacle test
  • the written testing and maintenance schedule for the system, with the log forms for each test NFPA 99 and NFPA 110 require of the Owner
  • the survey documentation set: the one-line, the branch load schedule, the classification statement, and the acceptance test records, bound or filed as the Authority Having Jurisdiction and the accrediting organization survey them
  • operation and maintenance data for each isolated power panel and line isolation monitor
  • the warranty documentation for the isolated power equipment and for the installation
  • a signed receipt from the Owner for the spare parts delivered
Closeout Submittalscheckbox
☑ As-built one-line diagram and branch load schedule
☑ Acceptance test records
☑ Testing and maintenance schedule with log forms
☑ Survey documentation set
☑ Isolated power operation and maintenance data
☑ Warranty documentation
☐ Spare parts receipt
NOTE The integrated acceptance test record under NFPA 110 Chapter 7 is delivered under Emergency And Standby PowerEmergency and Standby Power SystemsResolves to the current adopted revision.sync/emergency-and-standby-power; the records this standard requires are the branch-level and patient-care-level records that the integrated record does not contain. (3.3.2)

4 Quality Assurance

4.1 The essential electrical system one-line diagram, the branch load schedule, the classification statement, and the demand calculation shall be prepared by or under the responsible charge of a licensed Professional Engineer who has designed the essential electrical system of at least two health care facilities of the same type.
NOTE The risk category of each patient care space is determined by the facility's governing body under NFPA 99 Chapter 4, not by the Engineer of Record, and the engineer records it and designs to it; a category the engineer assumed without a written determination behind it is the finding a surveyor writes first. (4.2)
4.3 The Contractor shall engage, for the isolated power systems and the patient care receptacles, a testing firm that is independent of the installer and whose technicians have tested isolated power systems on at least two health care projects.
4.4 The reviews and the witnessing required for the essential electrical system shall be as indicated in the datasheet.
Reviews and Witnessing Requiredcheckbox
☐ State health department plan review before construction
☐ California HCAI review and inspection
☐ Accrediting organization survey documentation set
☑ Authority Having Jurisdiction witness of the acceptance test
NOTE A state health department or a state construction authority reviews the essential electrical system before construction in most states and inspects it before the facility is licensed, and the accrediting organization surveys the same records after occupancy; the reviews required on a project depend on the state and on whether the facility bills Medicare, so none is assumed beyond the witness every Authority Having Jurisdiction expects. (4.5)

5 Environmental and Service Conditions

5.1 The spaces that house the alternate source, the transfer switches, and the branch distribution equipment shall be located to minimize interruption of the essential electrical system by the natural hazards of the site, including storms, flooding, earthquakes, and hazards from adjoining structures or activities, in accordance with NFPA 70 517.30 and NFPA 99 Chapter 6.
5.2 No transfer switch or branch distribution equipment of the essential electrical system shall be installed below the design flood elevation of the site where the facility has space above it.
5.3 Where Seismic Design CategorySeismic Design CategoryParameterEach project supplies its own value.seismic-design-category is C or higher, the transfer switches, the branch distribution equipment, and the isolated power panels of the essential electrical system shall be treated as designated seismic systems with a component importance factor of 1.5 under ASCE/SEI 7, and the certification and anchorage of each item shall be furnished under the standard that governs it.
5.4 The alternate source shall be capable of restoring the life safety and critical branches within the time this standard requires at Site Ambient Temperature MinimumSite Ambient Temperature MinimumParameterEach project supplies its own value.site-ambient-temperature-minimum, with the engine readiness provisions furnished under GeneratorsEngine GeneratorsResolves to the current adopted revision.sync/generators.
NOTE Hospitals are Risk Category IV structures under the adopted building code, and the essential electrical system is the one system the building must still have when the event that cut the normal source is over, so the equipment that carries it is certified to keep working through the design earthquake rather than merely to stay anchored. (5.5)

6 System Classification

6.1 The health care facility type served by the system shall be as indicated in the datasheet.
Health Care Facility Typeselect
Hospital
Nursing home
Limited care facility
Ambulatory health care occupancy
Other health care facility with patient care spaces
NOTE The facility type decides which part of NFPA 70 Article 517 the system is built under. A hospital is built under the hospital provisions, which require the three-branch system whenever the facility has Category 1 spaces. A nursing home or a limited care facility is built under the provisions for those occupancies, which require a two-branch system, unless it admits residents who depend on electrical life support, in which case the hospital provisions apply. An ambulatory health care occupancy is built under NFPA 70 517.45, which requires an essential electrical system where the facility administers general anesthesia or uses electrical life support, and permits a battery system as the alternate source under the conditions it states. A medical office, a clinic, or an outpatient facility outside those occupancies is classified by the risk categories of its spaces alone. (6.2)
6.3 The highest risk category among the patient care spaces the system serves shall be as indicated in the datasheet.
Highest Risk Category of the Spaces Servedselect
Category 1
Category 2
Category 3
Category 4
Derived — the governing body's risk assessment under NFPA 99 Chapter 4 of every patient care space the system serves (by default)
NOTE NFPA 99 categorizes a space by what a failure of the system does to the patient in it, not by the name of the room: Category 1 where failure is likely to cause major injury or death, Category 2 where it is likely to cause minor injury, Category 3 where it causes discomfort but no injury, and Category 4 where it has no effect on patient care. An operating room, an intensive care unit, and a dialysis station are Category 1 almost everywhere; a general inpatient bed is Category 2 in most facilities and Category 1 where ventilator-dependent patients are housed; an examination room in a clinic is Category 3 or 4. (6.4)
6.5 The essential electrical system type shall be as indicated in the datasheet.
Essential Electrical System Typeselect
Type 1
Type 2
Type 3
No essential electrical system under NFPA 99
Derived — the highest risk category of the spaces served, with Type 1 for Category 1, Type 2 for Category 2, Type 3 for Category 3, and no essential electrical system under NFPA 99 where every space is Category 4 (by default)
6.6 A Type 1 system shall be divided into a life safety branch, a critical branch, and an equipment branch.
6.7 A Type 2 system shall be divided into a life safety branch and an equipment branch.
6.8 A Type 3 system shall have an alternate source, a battery system or a generator, capable of supplying the egress illumination and the alarm systems of the facility for not less than 1.5 hours.
NOTE The presence of one Category 1 space makes the system Type 1; the type is set by the most demanding space the system serves and not by how much of the facility that space represents. (6.9)
NOTE Where every space the system serves is Category 4, the facility still needs the emergency illumination and the alarm power the adopted building code and NFPA 101 require, and those are specified under Emergency And Standby PowerEmergency and Standby Power SystemsResolves to the current adopted revision.sync/emergency-and-standby-power and Emergency And Egress LightingEmergency and Egress LightingResolves to the current adopted revision.sync/emergency-and-egress-lighting without the provisions of this standard. (6.10)

7 Alternate Source of Power

7.1 The essential electrical system shall have at least two independent sources of power: the normal source that supplies the facility, and one or more alternate sources that supply the system when the normal source fails.
7.2 The alternate source type shall be as indicated in the datasheet.
Alternate Source Typeradio
● Engine-generator set on the premises
○ Second generating unit where the normal source is on-site generation
○ External utility service where the normal source is on-site generation
○ Battery system
○ Fuel cell system
NOTE An engine-generator set on the premises is the alternate source of nearly every health care facility, because it is the one source that carries the whole system for the runtime the facility plans for and that NFPA 110 classifies directly, which is why it is the default. The second generating unit and the external utility service are the alternate sources of a facility whose normal source is its own generation, a cogeneration plant or a remote campus, and each is accepted only because the normal source is already a generator. A battery system is limited to the facility types and the loads the adopted edition of NFPA 70 permits it for, and its runtime is set by its capacity rather than by a fuel delivery. A fuel cell system is a recent addition to the permitted sources and is accepted where the adopted edition includes it and the Authority Having Jurisdiction accepts the fuel supply arrangement. (7.3)
7.4 A battery system or a fuel cell system shall be the alternate source only where the adopted edition of NFPA 70 and NFPA 99 permit it for the facility type and the system type, and only where the Authority Having Jurisdiction has accepted it in writing before the classification statement is submitted.
7.5 A generator set serving the essential electrical system shall be classified Level 1, Type 10, Class X under NFPA 110, in accordance with NFPA 99 6.7, and shall be furnished under GeneratorsEngine GeneratorsResolves to the current adopted revision.sync/generators to that classification.
7.6 The runtime of the alternate source at the demand of the essential electrical system, which is the Class X duration, shall be as indicated in the datasheet.
Alternate Source Runtime at System Demandrange
Not less than
hours
246824487296120168
Derived — the runtime the facility's emergency management plan under NFPA 99 Chapter 12 establishes for the essential electrical system, and not less than the Authority Having Jurisdiction requires (by default)
NOTE NFPA 99 assigns Class X rather than a fixed class because the runtime is a planning decision of the facility: hospitals that plan to shelter in place through a regional event provision for 96 hours, which is the self-sufficiency period accrediting organizations ask a hospital to assess, while a facility that evacuates under its plan provisions for the time the evacuation takes. The runtime drives the fuel stored at the generator under GeneratorsEngine GeneratorsResolves to the current adopted revision.sync/generators and the fuel system beyond the skid under Fuel Oil SystemsFacility Fuel-Oil SystemsResolves to the current adopted revision.sync/fuel-oil-systems. (7.7)
7.8 The alternate source shall restore power to the life safety branch and the critical branch within 10 seconds of loss of the normal source, measured from the loss to the energization of the branch panelboards, with the engine start, the source acceptance, and the transfer switch delays all inside that time.
NOTE The 10 seconds is a system figure and not a per-component allowance: a generator that reaches voltage in 8 seconds behind a transfer switch with a 3 second transfer delay restores the branch in 11, so the restoration time budget submitted under this standard is the document in which the allowances are reconciled. (7.9)
7.10 The demand of the essential electrical system shall be computed on the basis indicated in the datasheet, in accordance with NFPA 70 517.31(D).
Essential Electrical System Demand Basisselect
Connected load
Feeder calculation under NFPA 70 Article 220
Prudent demand factors with the facility's historical data
Combination of the methods NFPA 70 517.31(D) permits
NOTE The connected load is the largest figure and the one a facility with no history uses when it would rather buy a larger set than defend a demand factor; the Article 220 feeder calculation applies the demand factors the code already grants and is the basis most new facilities use; prudent demand factors with historical data produce the smallest alternate source and are available only to an existing facility whose metered essential load over at least a year is in hand; and the combination lets each branch be calculated on the basis its data supports. The basis selected drives the alternate source capacity under Emergency And Standby PowerEmergency and Standby Power SystemsResolves to the current adopted revision.sync/emergency-and-standby-power and the set rating under GeneratorsEngine GeneratorsResolves to the current adopted revision.sync/generators. (7.11)
7.12 Where the facility has more than one alternate source, the sources shall be arranged so that the life safety and critical branches remain supplied on the loss of any one source, with the redundancy and the paralleling scheme selected under Emergency And Standby PowerEmergency and Standby Power SystemsResolves to the current adopted revision.sync/emergency-and-standby-power and furnished under Generator Paralleling SwitchgearGenerator Paralleling SwitchgearResolves to the current adopted revision.sync/generator-paralleling-switchgear.

8 Branch Structure and Load Assignment

8.1 The branch assignment of each load shall be as indicated on the panel schedules and the essential electrical system branch load schedule.
NOTE The branches exist so that the loads a patient's life depends on in the next ten seconds, the loads the clinical staff need to keep treating, and the building equipment that keeps the facility habitable are supplied through separate transfer switches and separate wiring, so that a fault, an overload, or a maintenance outage on one of them leaves the others energized. (8.2)

8.3 Life Safety Branch

8.3.1 The life safety branch shall supply only the loads NFPA 70 517.32 lists for it: the illumination of the means of egress, the exit signs, the fire alarm and the medical gas alarms, the communication systems used to issue instructions in an emergency, the task illumination, the battery charger, and the selected receptacles at the generator set and the transfer switch locations, the elevator cab lighting, control, communication, and signal systems, and the automatic doors used for egress.
8.3.2 No load other than those NFPA 70 517.32 lists shall be connected to the life safety branch.
8.3.3 The life safety branch shall meet NFPA 70 Article 700 as NFPA 70 517.26 applies it, with the amendments Article 517 makes to it.
NOTE The life safety branch is the branch most often overloaded by design rather than by use, because a nurse station, a security desk, or a data closet reads as life safety to the people who work there and none of them is on the list; the list is exclusive, and a load that is not on it belongs on the critical or the equipment branch. (8.3.4)
8.3.5 The egress illumination and the exit signs the life safety branch supplies shall be specified under Emergency And Egress LightingEmergency and Egress LightingResolves to the current adopted revision.sync/emergency-and-egress-lighting, the fire alarm system under Fire Alarm SystemsFire Alarm SystemsResolves to the current adopted revision.sync/fire-alarm-systems, and the medical gas alarm panels under Medical Gas SystemsMedical Gas and Vacuum SystemsResolves to the current adopted revision.sync/medical-gas-systems, each with its branch circuit assigned to the life safety branch.

8.4 Critical Branch

8.4.1 The critical branch shall supply the task illumination, the fixed equipment, the selected receptacles, and the selected power circuits of the patient care spaces and the clinical support functions NFPA 70 517.33 lists, and the isolated power systems this standard requires.
8.4.2 The nurse call system specified under Nurse Call SystemsNurse Call SystemsResolves to the current adopted revision.sync/nurse-call-systems shall be supplied from the critical branch.
8.4.3 The critical branch shall be permitted to be subdivided into two or more branches, each served by its own transfer switch, in accordance with NFPA 70 517.33.
NOTE The critical branch of a large hospital is routinely split by floor, by wing, or by service into several branches on separate transfer switches, because a single critical branch transfer switch becomes the one device whose failure darkens every patient care space at once, and because a split lets a floor be taken down for maintenance without touching the others. (8.4.4)
8.4.5 Each patient bed location, each operating room, and each procedure room shall be supplied from the critical branch in the manner the Patient Care Space Circuits and Receptacles section of this standard requires.

8.5 Equipment Branch

8.5.1 The equipment branch shall supply the three-phase and the building equipment NFPA 70 517.34 lists: the central suction and the medical air compressors, the sump pumps, the smoke control and stair pressurization fans, the kitchen hood fans required to run during a fire, the supply, return, and exhaust systems of airborne infection isolation rooms, protective environment rooms, operating rooms, and the other spaces 517.34 names, the heating of the patient care spaces it names, the elevators selected to serve patient, surgical, obstetrical, and ground floors, the sterilizers, and the controls of that equipment.
8.5.2 The equipment NFPA 70 517.34(A) lists shall be connected to the alternate source by delayed automatic connection.
8.5.3 The equipment NFPA 70 517.34(B) lists shall be connected to the alternate source in the manner indicated in the datasheet.
Connection of NFPA 70 517.34(B) Equipmentradio
● Delayed automatic connection
○ Manual connection by the operator
NOTE Delayed automatic connection is the manner nearly every facility selects for the heating, the ventilation, and the elevators 517.34(B) permits to be connected manually, because an operator who must walk to a transfer switch during an outage is an operator the clinical staff do not have, which is why it is the default; manual connection is selected where the equipment would overload the alternate source unless the operator first confirms the load it carries. (8.5.4)
8.5.5 The generator accessories that the alternate source needs to run, including the fuel transfer pumps, the electrically operated louvers, and the ventilation of the generator room, shall be connected to the alternate source without delay, in accordance with NFPA 70 517.34.
8.5.6 The heating of general patient rooms shall be supplied from the equipment branch unless Site Ambient Temperature MinimumSite Ambient Temperature MinimumParameterEach project supplies its own value.site-ambient-temperature-minimum is above -6.7°C (20°F) or another condition of the exception to NFPA 70 517.34(B)(1) is met and documented in the branch load schedule.
8.5.7 The supply, return, and exhaust systems of airborne infection isolation rooms and protective environment rooms shall be supplied from the equipment branch by delayed automatic connection, with the air systems themselves specified under Air Handling UnitsAir Handling UnitsResolves to the current adopted revision.sync/air-handling-units and HVAC FansHVAC FansResolves to the current adopted revision.sync/hvac-fans and the ventilation requirement under ANSI/ASHRAE/ASHE 170.
8.5.8 The smoke control and stair pressurization fans specified under Smoke Control SystemsSmoke Control SystemsResolves to the current adopted revision.sync/smoke-control-systems and the kitchen hood fans specified under Kitchen Exhaust SystemsKitchen Exhaust SystemsResolves to the current adopted revision.sync/kitchen-exhaust-systems that the adopted building code requires to operate during a fire shall be supplied from the equipment branch by delayed automatic connection.
8.5.9 The equipment branch wiring shall be permitted to occupy the same raceways, boxes, and cabinets as wiring that is not part of the essential electrical system, in accordance with NFPA 70 517.31(C)(1).
NOTE The equipment branch is where the alternate source is sized and where it is overloaded: the chillers, the air handlers, and the elevators it carries are the large motors of the building, and the delay before they connect exists so that the life safety and critical branches are energized and the set is stable before the first of them starts. (8.5.10)

9 Transfer Switches of the Essential Electrical System

9.1 Each branch of the essential electrical system shall be served by one or more transfer switches, in accordance with NFPA 70 517.31(B), with the switches themselves furnished under Automatic Transfer SwitchesAutomatic Transfer SwitchesResolves to the current adopted revision.sync/automatic-transfer-switches.
9.2 The transfer switch arrangement shall be as indicated in the datasheet.
Transfer Switch Arrangementradio
○ One transfer switch per branch
○ Several transfer switches per branch
○ One transfer switch for the whole essential electrical system
NOTE One transfer switch per branch is the arrangement NFPA 70 517.31(B) describes and the one a facility of moderate size builds; several transfer switches per branch is the arrangement of a hospital whose critical branch is split by floor or by service and whose equipment branch is sequenced across several switches with staggered delays; and one transfer switch for the whole system is permitted only to a facility whose essential electrical system demand does not exceed 150 kVA, which is a small nursing home or an ambulatory facility, and it buys one switch at the cost of every branch sharing one point of failure. (9.3)
9.4 One transfer switch shall serve more than one branch only where the maximum demand of the essential electrical system does not exceed 150 kVA (120 kW).
9.5 The bypass-isolation provision of the transfer switches serving the essential electrical system shall be as indicated in the datasheet, and shall be furnished on each switch under Automatic Transfer SwitchesAutomatic Transfer SwitchesResolves to the current adopted revision.sync/automatic-transfer-switches.
Bypass-Isolation on Essential Electrical System Transfer Switchesradio
○ Bypass-isolation on every transfer switch of the system
○ Bypass-isolation on the life safety and critical branch transfer switches
○ No bypass-isolation
NOTE Bypass-isolation on every switch lets any switch be inspected, tested, or replaced with its branch energized, which in a hospital is the difference between a maintenance task and a patient relocation, and it is the arrangement of most acute care facilities; bypass-isolation on the life safety and critical branch switches alone keeps that capability where an outage reaches the patient and accepts a scheduled outage of the building equipment; and no bypass-isolation is the arrangement of a facility that can take each branch down on a schedule, which a nursing home or an outpatient facility often can. Neither NFPA 70 nor NFPA 99 requires bypass-isolation, so the selection is the facility's, and the cost of every switch roughly doubles with it. (9.6)
9.7 The connection sequence of the equipment branch shall be as indicated in the datasheet.
Equipment Branch Connection Sequenceradio
○ One delayed step for the whole equipment branch
○ Sequenced steps on separate transfer switches with staggered delays
○ Load added by the paralleling switchgear priority table
NOTE One delayed step connects the whole equipment branch at one transfer switch after one delay, which suits a facility whose equipment branch is small relative to the set; sequenced steps on separate transfer switches, each with its own delay, bring the equipment branch on in increments the set can accept and are the arrangement of a hospital with a single set or a few sets on individual switches; and load added by the paralleling switchgear priority table hands the sequence to the lineup furnished under Generator Paralleling SwitchgearGenerator Paralleling SwitchgearResolves to the current adopted revision.sync/generator-paralleling-switchgear, which adds each block as capacity comes on line and sheds it in reverse when a set is lost. The sequence and the delays are the inputs to the step-load analysis the set manufacturer performs under GeneratorsEngine GeneratorsResolves to the current adopted revision.sync/generators. (9.8)
9.9 The time delay of each equipment branch transfer switch shall be set so that the life safety and critical branches are energized before the first equipment branch step connects, and the delays as commissioned shall be recorded in the acceptance test records.
9.10 The transition type, the neutral treatment, and the time delays of each transfer switch shall be selected under Emergency And Standby PowerEmergency and Standby Power SystemsResolves to the current adopted revision.sync/emergency-and-standby-power and Automatic Transfer SwitchesAutomatic Transfer SwitchesResolves to the current adopted revision.sync/automatic-transfer-switches, and no transfer switch of the essential electrical system shall carry a transition type or a neutral treatment that differs from the one those standards select for the system.

10 Wiring of the Essential Electrical System

10.1 The wiring of the life safety branch and of the critical branch shall be kept entirely independent of all other wiring and equipment, and shall not enter the same raceway, box, or cabinet as each other or as any other wiring, except at the points NFPA 70 517.31(C)(1) permits: inside transfer switch enclosures, inside an exit or emergency luminaire supplied from two sources and the junction box attached to it, and where two or more circuits are supplied from the same branch and the same transfer switch.
10.2 The wiring of the life safety branch and of the critical branch shall be mechanically protected by installation in one of the wiring methods indicated in the datasheet, in accordance with NFPA 70 517.31(C)(3), with the raceway products furnished under Raceways And ConduitRaceways and ConduitResolves to the current adopted revision.sync/raceways-and-conduit and the cable under Conductors And CablesConductors and CablesResolves to the current adopted revision.sync/conductors-and-cables.
Life Safety and Critical Branch Wiring Methods Permittedcheckbox
Any of:
☑ Nonflexible metal raceway
☐ Type MI cable
☐ Schedule 80 PVC conduit for feeders
☐ Schedule 40 PVC conduit or other listed raceway encased in 50 mm of concrete
NOTE Nonflexible metal raceway, meaning rigid metal conduit, intermediate metal conduit, or electrical metallic tubing, is the method of nearly every life safety and critical branch run inside the building, because it is the one method that satisfies the mechanical protection rule and the redundant grounding rule of patient care spaces at once, which is why it is the only method selected by default; Type MI cable is selected where a feeder must survive fire exposure or where a raceway cannot be run; Schedule 80 PVC conduit is permitted for feeders and is the method of an exposed exterior run, and it is never permitted for a branch circuit that supplies a patient care space; and Schedule 40 PVC conduit encased in concrete is the method of the underground feeders between a generator building and the facility. (10.3)
10.4 No nonmetallic raceway shall be used for a branch circuit that supplies a patient care space.
10.5 Listed flexible metal raceway and listed metal-sheathed cable shall be used for the life safety and critical branches only inside listed prefabricated medical headwalls, inside listed office furnishings, where fished into an existing wall or ceiling that is not otherwise accessible and not subject to physical damage, and where a flexible connection to equipment is necessary, in accordance with NFPA 70 517.31(C)(3).
10.6 Each isolated power system shall be supplied by an individual circuit from the critical branch that serves no other load, in accordance with NFPA 70 517.31(C)(2).
10.7 The feeders of the life safety branch and of the critical branch shall be routed so that no single fire, flood, or physical event in one space can disable more than one branch, with the routing as indicated on the essential electrical system riser diagram.
NOTE The separation rule is the reason the branches survive: a critical branch feeder that shares a pull box with the normal feeder it parallels is a feeder that burns with it, and the inspector who opens the box after the fire is the one who finds the shared enclosure. (10.8)

11 Patient Care Space Circuits and Receptacles

11.1 Each patient bed location in a Category 1 or a Category 2 space shall be supplied by at least two branch circuits arranged as indicated in the datasheet, in accordance with NFPA 70 517.18(A) and 517.19(A).
Patient Bed Location Branch Circuit Sourcesradio
● At least one normal system circuit and at least one critical branch circuit
○ Critical branch circuits from two separate transfer switches
NOTE One normal system circuit and one critical branch circuit at each bed is the arrangement NFPA 70 Article 517 states and the one nearly every facility builds, because the normal circuit stays energized through a failure of the essential electrical system itself, which is why it is the default; critical branch circuits from two separate transfer switches is the exception the article permits where the facility would rather have every bed on the essential system, and it is selected only where the two transfer switches are fed by separate feeders so that neither failure darkens the bed. (11.2)
11.3 Each patient bed location in a Category 1 space shall be supplied by at least one critical branch circuit that serves no other bed location.
11.4 The number of receptacles at each patient bed location in a Category 2 general care space shall be as indicated in the datasheet, in accordance with NFPA 70 517.18(B).
Receptacles at a General Care Patient Bed Locationrange
Not less than
receptacles
824
Default: 8 receptacles
11.5 The number of receptacles at each patient bed location in a Category 1 critical care space shall be as indicated in the datasheet, in accordance with NFPA 70 517.19(B).
Receptacles at a Critical Care Patient Bed Locationrange
Not less than
receptacles
1448
Default: 14 receptacles
11.6 At least one receptacle at each critical care patient bed location shall be supplied from the normal system or from a critical branch circuit on a different transfer switch from the others at that bed.
11.7 The number of receptacles in each operating room shall be as indicated in the datasheet, in accordance with NFPA 70 517.19(C).
Receptacles in an Operating Roomrange
Not less than
receptacles
3672
Default: 36 receptacles
11.8 At least 12 of the receptacles in each operating room shall be supplied from the normal system or from a critical branch circuit on a different transfer switch from the others in the room.
NOTE The counts the datasheet defaults to are the floors NFPA 70 Article 517 sets, and a receptacle counts toward them whether it is a single, a duplex counted as two, or a quadruplex counted as four; a headwall or a boom in an intensive care room and an equipment-dense operating room both run well above the floor, and the count the facility wants is settled with the clinical planner against the equipment list, not against the code. (11.9)
11.10 Every receptacle at a patient bed location and in an operating room shall be a listed hospital-grade receptacle furnished under Wiring DevicesWiring DevicesResolves to the current adopted revision.sync/wiring-devices, with the count this standard requires and the grade that standard requires for the space.
11.11 Receptacles in the patient care spaces of a pediatric location shall be listed tamper-resistant receptacles or shall be installed behind a listed tamper-resistant cover, in accordance with NFPA 70 517.18(C), with the device furnished under Wiring DevicesWiring DevicesResolves to the current adopted revision.sync/wiring-devices.
11.12 No isolated-ground receptacle shall be installed within the patient care vicinity of a patient care space, in accordance with NFPA 70 517.16.
11.13 The receptacles and the cover plates of the life safety branch and of the critical branch shall be identified in the manner indicated in the datasheet so that they are readily distinguishable from the receptacles of the normal system, in accordance with NFPA 70 517.31(E).
Life Safety and Critical Branch Receptacle Identificationcheckbox
☑ Distinctive color of the receptacle face
☐ Distinctive color of the cover plate
☐ Branch name on the cover plate
☑ Panelboard designation and circuit number on the cover plate
11.14 Where the datasheet selects a distinctive color, the color shall be red unless Electrical IdentificationWiring System IdentificationResolves to the current adopted revision.sync/electrical-identification assigns the essential electrical system another color, and the same color shall identify the branch receptacles throughout the facility.
11.15 Where the datasheet selects the panelboard designation and circuit number, each receptacle of the life safety and critical branches in a patient care space shall carry them on its cover plate in characters legible from the bed.
NOTE A red face is the identification a clinician recognizes without reading, and it is the convention of nearly every facility in the country, which is why it is the default; a red cover plate on a general-color device is selected where the facility has standardized on one device color; the branch name on the plate tells the clinician which branch the outlet is on, which matters where both branches serve one room; and the panelboard and circuit number on the plate is what lets the staff and the electrician find the breaker for the outlet a device is plugged into without leaving the room, which is why it is in the default alongside the color. (11.16)
11.17 The grounding of every patient care space shall be the redundant grounding NFPA 70 517.13 requires, and the grounding test NFPA 99 requires of the space shall be performed, both under Grounding And BondingGrounding and Bonding for Electrical SystemsResolves to the current adopted revision.sync/grounding-and-bonding.

12 Ground-Fault Protection

12.1 Where ground-fault protection of equipment is provided on the service disconnecting means or on a feeder disconnecting means of a facility that NFPA 70 517.17(A) applies to, an additional level of ground-fault protection shall be provided in the next level of feeder disconnecting means downstream toward the load, in accordance with NFPA 70 517.17(B), and the provision shall be as indicated in the datasheet.
Second Level of Ground-Fault Protection of Equipmentselect
Second level of ground-fault protection provided
Not applicable, no ground-fault protection on the service or feeder disconnecting means
Derived — whether the service disconnecting means or a feeder disconnecting means of the facility carries ground-fault protection of equipment under NFPA 70 230.95 or 215.10 (by default)
NOTE The second level exists so that a ground fault on one feeder opens that feeder and not the service: a hospital with a single level of ground-fault protection on a 2000 A service loses the whole building, essential system included until the transfer switches see the loss, to a fault in one panelboard. The requirement is triggered by the first level, which NFPA 70 230.95 requires on a solidly grounded wye service of 1000 A and more at more than 150 V to ground, so a facility served at 480Y/277 V above that size has it and a facility served at 208Y/120 V does not. (12.2)
12.3 No ground-fault protection of equipment shall be installed on the load side of a transfer switch of the essential electrical system.
12.4 The two levels of ground-fault protection shall be fully selective, so that a ground fault on the load side of a feeder device opens that device and not the service device, with a separation of not less than six cycles between the time-current characteristics of the two levels, in accordance with NFPA 70 517.17(C).
12.5 The pickup of the second level of ground-fault protection shall be as indicated in the datasheet, and no level shall be set in the field to a value the coordination study does not record.
Second-Level Ground-Fault Pickuprange
A
10020030040050060080010001200
Derived — the pickup the coordination study under [[sync/protective-coordination-study]] assigns to the feeder level, below the service level pickup and above the leakage and unbalance current of the feeder (by default)
12.6 The time delay of the second level of ground-fault protection shall be as indicated in the datasheet.
Second-Level Ground-Fault Time Delayrange
s
0.10.20.30.40.5
Derived — the time delay the coordination study under [[sync/protective-coordination-study]] assigns to the feeder level, not less than six cycles below the service level delay (by default)
12.7 Each level of ground-fault protection shall be performance tested when first installed, by primary current injection or by the method the study and the equipment manufacturer accept, and a written record of the test shall be delivered under the closeout submittals, in accordance with NFPA 70 517.17(D).

13 Isolated Power Systems

13.1 The governing body shall designate the wet procedure locations of the facility under NFPA 99 Chapter 6, and the protection of the circuits in each wet procedure location shall be as indicated in the datasheet, in accordance with NFPA 70 517.20.
Wet Procedure Location Protectionradio
○ Isolated power system
○ Ground-fault circuit-interrupter protection
Derived — the governing body's determination under NFPA 99 Chapter 6 of whether interruption of power on a first ground fault is tolerable in each wet procedure location (by default)
NOTE NFPA 99 treats an operating room as a wet procedure location unless the governing body's risk assessment finds otherwise, and the two protections it allows answer different questions: ground-fault circuit-interrupter protection opens the circuit on the first fault, which protects the patient by de-energizing the equipment, and an isolated power system alarms on the first fault and keeps the circuit energized, which protects the patient by keeping the equipment running. The isolated power system is selected where the interruption would be worse than the fault, which is the case in a room where a device is keeping the patient alive, and ground-fault protection is selected where the interruption is tolerable. (13.2)
13.3 Each isolated power system shall be a listed assembly under UL 1047 comprising an isolation transformer, a line isolation monitor listed under UL 1022, the secondary overcurrent devices, and the receptacles and their wiring, installed in accordance with NFPA 70 517.160.
13.4 The isolation transformer of each isolated power system shall be a dry-type transformer built for the isolated power panel, with an ungrounded secondary, an electrostatic shield between the primary and secondary windings connected to the reference grounding point, and a leakage current from the secondary to ground, with the monitor disconnected, low enough that the total hazard current of the installed system at no load does not exceed the monitor's margin, and it shall be furnished as part of the UL 1047 assembly rather than under Low Voltage Dry Type TransformersLow-Voltage Dry-Type TransformersResolves to the current adopted revision.sync/low-voltage-dry-type-transformers.
13.5 The transformer rating of each isolated power panel shall be as indicated in the datasheet.
Isolated Power Panel Transformer Ratingrange
kVA
357.5101525
Per drawings — the isolated power panel schedule (deferred by default)
13.6 The secondary voltage of each isolated power panel shall be as indicated in the datasheet.
Isolated Power Panel Secondary Voltageselect
120 V, 1Φ
208 V, 1Φ
240 V, 1Φ
208 V, 3Φ
NOTE A 120 V single-phase secondary serves the receptacles and the equipment of nearly every operating room and procedure room, which is why it is the default; a 208 V or a 240 V single-phase secondary serves a specific device, an imaging unit, a laser, or a hyperbaric chamber, that needs it, and is furnished as a second isolated system rather than by converting the receptacle system; and a 208 V three-phase secondary serves a three-phase device, and its third conductor takes the third identification color. (13.7)
13.8 The conductors of each isolated system shall be identified by the colors NFPA 70 517.160(A) assigns: orange for the first isolated conductor, brown for the second, and yellow for the third of a three-phase system, each with the distinctive stripe the adopted edition requires.
13.9 The conductors of each isolated system shall have insulation with a dielectric constant not greater than 3.5, and the wiring between the panel and its receptacles shall be the shortest practicable length, so that the capacitive leakage of the wiring leaves the monitor its hazard current margin.
13.10 The line isolation monitor of each isolated power system shall indicate a total hazard current that does not exceed 5 mA by a green signal and shall alarm by a red signal and an audible signal when the total hazard current reaches 5 mA, and shall not alarm at a fault hazard current below 3.7 mA, in accordance with NFPA 70 517.160(B).
13.11 The line isolation monitor shall have an ammeter reading the total hazard current, mounted where it is visible from the procedure room, and a test switch that produces an alarm without introducing a fault into the system.
13.12 The indication furnished for each line isolation monitor shall be as indicated in the datasheet.
Line Isolation Monitor Indicationcheckbox
☑ Indicator on the isolated power panel
☑ Remote indicator in the procedure room
☐ Alarm contact to the nurse call or clinical alarm system
☐ Status point to the building management system
NOTE The indicator on the panel is integral to the monitor and the remote indicator is what the staff in the room actually see, because the panel is usually in the corridor or behind the control desk, which is why both are in the default; the alarm contact carries the alarm to the staff station through Nurse Call SystemsNurse Call SystemsResolves to the current adopted revision.sync/nurse-call-systems where the facility wants the alarm answered by someone outside the room; and the status point lets the facility trend hazard current and log alarms, at the cost of a controls interface at each panel. (13.13)
13.14 The enclosure type of each isolated power panel shall be as indicated in the datasheet.
Isolated Power Panel Enclosure Typeselect
Type 1
Type 12
Type 4X
NOTE Type 1 is the enclosure of a panel installed in a finished procedure room, a corridor, or an equipment room, which is where nearly every panel is installed, which is why it is the default; Type 12 is selected in a sterile processing or a laboratory space where dust and dripping liquid reach the panel; and Type 4X in stainless steel is selected where the panel is in a space that is washed down. (13.15)
13.16 Where an isolated power panel is installed in a space that is washed down or exposed to a corrosive atmosphere, its enclosure shall be Type 4X.
13.17 The mounting of each isolated power panel shall be as indicated in the datasheet.
Isolated Power Panel Mountingradio
● Flush
○ Surface
NOTE A flush panel sits in the wall of the operating room with its face in the finish, which is the installation of nearly every new operating room because the room is cleaned to the wall, which is why it is the default; a surface panel is selected in an existing wall that cannot be opened, in an equipment room, or where the room design places the panel outside the sterile field. (13.18)
13.19 The receptacles of each isolated power system shall be listed hospital-grade receptacles furnished under Wiring DevicesWiring DevicesResolves to the current adopted revision.sync/wiring-devices, identified as isolated power receptacles, and supplied by no circuit other than the isolated system that serves the room.

14 Selective Coordination

14.1 The overcurrent protective devices serving the essential electrical system shall be coordinated for the period of time that a fault's duration extends beyond 0.1 second, in accordance with NFPA 70 517.31(G), with the exceptions that section states for the devices between a transformer primary and secondary and for devices of the same size in series.
14.2 The coordination shall be demonstrated by the study prepared under Protective Coordination StudyProtective Device Coordination StudyResolves to the current adopted revision.sync/protective-coordination-study, which governs the method, the devices and settings it recommends, and the deliverables, and the study shall be completed before any overcurrent device of the essential electrical system is procured.
NOTE NFPA 70 Article 517 amends the full-range coordination Article 700 requires of an emergency system to coordination beyond 0.1 second for the whole essential electrical system, so a pair of molded-case breakers that overlap in the instantaneous region, which would fail under Article 700, coordinates under Article 517; a project whose Authority Having Jurisdiction applies a different boundary records that boundary in the study under Emergency And Standby PowerEmergency and Standby Power SystemsResolves to the current adopted revision.sync/emergency-and-standby-power. (14.3)

15 Identification and Documentation

15.1 Each transfer switch, each branch panelboard and distribution board, and each feeder raceway and junction box of the essential electrical system shall be identified by the branch it serves, with the nameplate and the marking furnished under Equipment LabelingElectrical Equipment LabelsResolves to the current adopted revision.sync/equipment-labeling.
15.2 The boxes and enclosures of the life safety branch shall be permanently marked as components of the emergency system, in accordance with NFPA 70 700.10(A) as Article 517 applies it.
15.3 The Contractor shall maintain, through construction and into the closeout submittals, a single branch load schedule in which every change of branch assignment is entered with its date and the provision that supports it.
15.4 The survey documentation set delivered under the closeout submittals shall be organized so that a surveyor can trace any patient care space from its risk category to its branch, its transfer switch, its alternate source, and the acceptance test record that proves its restoration time.
NOTE The documents a state surveyor and an accrediting organization ask for at every survey are the same four: the one-line, the branch load schedule, the classification statement, and the test records; a facility that hands them over in one binder, or one folder, finishes the electrical portion of the survey in an hour, and a facility that has to assemble them from shop drawings does not. (15.5)

16 Testing

16.1 Acceptance Testing

16.1.1 The Contractor shall perform the acceptance tests indicated in the datasheet on the essential electrical system before it is placed in service, with each test witnessed as the Quality Assurance section requires and recorded as the closeout submittals require.
Essential Electrical System Acceptance Testscheckbox
☑ Restoration time of each branch measured from loss of the normal source
☑ Equipment branch connection sequence and time delays
☑ Ground-fault protection performance test under NFPA 70 517.17(D)
☑ Isolated power system and line isolation monitor tests
☑ Patient care receptacle tests under NFPA 99
☑ Integrated system test under NFPA 110 Chapter 7
16.1.2 The restoration time of the life safety branch and of the critical branch shall be measured at the branch panelboards on a loss of the normal source simulated at the service, and no branch shall be accepted whose measured restoration time exceeds 10 seconds.
16.1.3 The connection sequence and the time delay of each equipment branch transfer switch shall be verified against the sequence the datasheet selects and the delays the acceptance test records state.
16.1.4 Each isolated power system shall be tested after installation and before it is placed in service by measuring the impedance to ground of each isolated conductor, which shall exceed 200 kΩ, by verifying that the line isolation monitor alarms at the hazard current this standard requires and not below 3.7 mA, and by operating the test switch and each remote indicator and alarm contact, in accordance with NFPA 99 6.3.
16.1.5 Each receptacle in a patient care space shall be tested after installation for physical integrity, for correct polarity, for continuity of the grounding contact, and for a retention force on the grounding blade of not less than 115 g (4 oz), in accordance with NFPA 99 6.3, and each receptacle that fails shall be replaced and retested at the Contractor's cost.
16.1.6 The integrated system test under NFPA 110 Chapter 7 shall be performed under Emergency And Standby PowerEmergency and Standby Power SystemsResolves to the current adopted revision.sync/emergency-and-standby-power and scheduled so that the branch restoration tests of this standard are performed during it.
16.1.7 The patient care grounding test NFPA 99 requires shall be performed under Grounding And BondingGrounding and Bonding for Electrical SystemsResolves to the current adopted revision.sync/grounding-and-bonding before the receptacle tests of this standard, so that a receptacle is tested against a grounding path that has already been proven.
NOTE The retention force test is the one that fails most often, because a receptacle that has had a construction cord pulled from it a few hundred times no longer holds a plug, and a plug that falls out of a receptacle on the critical branch is the failure the branch cannot protect against. (16.1.8)

16.2 Supplemental Load for Testing

16.2.1 The supplemental load provision for testing the alternate source of the essential electrical system shall be as indicated in the datasheet.
Supplemental Load Provision for Testingradio
○ Permanently installed load bank
○ Load bank connection for a portable load bank
○ No supplemental load provision
NOTE A permanently installed load bank lets the facility reach the loading NFPA 110 requires of every monthly test without bringing anything to the site, and it is selected where the building load on the essential system is a small fraction of the set rating, which is the case at a facility whose equipment branch is small or whose sets are redundant; a load bank connection accepts a rented load bank for the annual and the 36-month tests and costs a cabinet and a feeder, and it is the provision of most facilities whose monthly building load is adequate; and no provision is selected where the building load on the system reaches the required loading every month, which the facility proves from its own logs rather than assumes. The load bank, where permanent, is furnished under GeneratorsEngine GeneratorsResolves to the current adopted revision.sync/generators with the set it tests. (16.2.2)
16.2.3 The rating of the permanently installed load bank, where the datasheet selects one, shall be as indicated in the datasheet.
Permanent Load Bank Ratingrange
kW
5010015020030040050075010001500200025003000
Per drawings — the one-line diagram (deferred by default)
16.2.4 Where a permanently installed load bank is furnished, it shall be connected so that it is shed automatically when the normal source fails during a test, so that no test ever reduces the capacity available to the branches.

16.3 Periodic Testing Program

16.3.1 The Contractor shall deliver to the Owner, as a closeout submittal, a written testing and maintenance program for the essential electrical system that documents the elements indicated in the datasheet, with the interval, the acceptance criterion, and the log form for each, in accordance with NFPA 99 Chapter 6 and NFPA 110 Chapter 8.
Periodic Testing Program Elements Documentedcheckbox
☑ Generator test twelve times a year at intervals of 20 to 40 days for 30 minutes under load
☑ Annual supplemental load test where the monthly loading is not reached
☑ Four-hour load test once in every 36 months
☑ Monthly operation of every transfer switch
☑ Monthly line isolation monitor test and annual hazard current verification
☑ Patient care receptacle testing at the intervals NFPA 99 sets
☑ Weekly inspection of the alternate source and its starting batteries
16.3.2 The program shall state that the monthly generator test is performed at not less than 30 percent of the nameplate rating of the set or at a loading that reaches the exhaust gas temperature the engine manufacturer recommends, and that where neither is reached, the annual supplemental load test is performed at the loadings and for the durations NFPA 110 Chapter 8 states.
16.3.3 The program shall state the receptacle testing intervals NFPA 99 sets for the facility, which are shorter for receptacles in Category 1 spaces and for receptacles that are not hospital-grade, and shall identify every receptacle on the program by room and by branch.
NOTE The Owner performs the periodic tests, and the program the Contractor delivers is what the Owner's staff and the surveyor both read: a surveyor asks for the log of the last twelve generator tests and the last twelve transfer switch operations, and a facility whose program names the interval, the loading, and the form has a log to show. (16.3.4)

17 Installation

17.1 The transfer switches, the branch panelboards and distribution boards, and the isolated power panels of the essential electrical system shall be installed where indicated on the electrical plans, in the spaces the Environmental and Service Conditions section of this standard requires.
17.2 The isolated power panel of each wet procedure location shall be installed where indicated on the procedure room power plans, with its remote indicator in the line of sight of the staff at the procedure table.
17.3 Where the work is performed in an operating health care facility, the existing essential electrical system shall remain in service throughout, and every planned interruption of a branch shall be scheduled with the facility in writing not less than 14 days before it occurs, with the interim measures the facility's life safety and infection control procedures require in place before the interruption begins.
17.4 No branch of an existing essential electrical system shall be interrupted for connection of new work until the facility has confirmed in writing that every patient care space the branch serves has been provided for during the interruption.
17.5 The branch assignment of every circuit shall be verified against the branch load schedule at the panelboard before the circuit is energized, and a circuit found on a branch the schedule does not assign it to shall be moved before energization.
17.6 The feeders of the life safety and critical branches shall be installed in the separate routes the riser diagram shows, and no feeder of either branch shall be rerouted through an enclosure or a chase that another branch or the normal system occupies without the Engineer of Record's written acceptance.
NOTE The interruption a renovation causes is the most common way an operating hospital loses its essential electrical system: not a utility failure, but an electrician opening a critical branch panelboard to add a circuit without knowing which beds it served. The schedule, the notice, and the written confirmation exist to make that impossible. (17.7)

18 Warranty

18.1 The manufacturer shall warrant each isolated power panel and line isolation monitor against defects in materials and workmanship for the period indicated in the datasheet, measured from the date of substantial completion.
Isolated Power Equipment Warranty Periodrange
Not less than
years
1235
18.2 Where the contract documents state a longer warranty period than the datasheet, the longer period shall govern.
18.3 The Contractor shall warrant the installation of the essential electrical system, including the branch separation, the branch assignment of every circuit, the receptacle identification, and the commissioned restoration time of each branch, for the project warranty period.
18.4 A repair or replacement performed under this warranty shall itself be warranted for a full new term equal to the original period from the date the repair is completed, or for the remainder of the original period, whichever ends later.
NOTE The warranties of the transfer switches, the generator sets, and the paralleling switchgear are made under their own standards; this warranty covers the system work those standards do not, which is the work that decides whether the branches do what the classification statement says they do. (18.5)

19 Spare Parts

19.1 The Contractor shall deliver the spare parts indicated in the datasheet to the Owner before the essential electrical system is accepted, and shall obtain a signed receipt for them.
Spare Parts to Be Furnishedcheckbox
☑ One line isolation monitor of each type furnished
☐ One remote indicator of each type furnished
☐ One set of secondary fuses for each isolated power panel type
☐ One isolated power receptacle of each configuration furnished
☑ Keys for every lock furnished
19.2 Spare parts shall be of the same manufacturer and rating as the installed items, shall be delivered in their original packaging, and shall be labeled with the designation of the panel they serve.
19.3 The Owner's facility staff shall be trained on the essential electrical system for the period indicated in the datasheet, covering the branches and the spaces each serves, the transfer switch arrangement, the equipment branch sequence, the isolated power systems and their monitors, the periodic testing program, and the records a surveyor asks for.
Facility Staff Training Periodrange
Not less than
hours
24816

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"Healthcare Essential Electrical Systems," SynC Standards, revision 4. Licensed under CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/). Source: https://synergyinconstruction.com/standards/general/healthcare-essential-electrical-systems. Reference material only; not professional engineering advice and provided without warranty. Verify against governing codes and have a licensed professional review before use.