Body Protected Areas (BPA):
1. Inspector qualification & scope
An inspector doing a BPA must:
Be competent in the patient-area / medical-electrical arena: testing of RCDs, knowledge of equipotential bonding, shock hazard control in patient environments.
The installation falls under “intended for use with electrical medical devices” and is a high-risk installation under Electricity (Safety) Regulations 2010 — hence inspection/verification is required.
Know the relevant standards: AS/NZS 3000 (Wiring Rules) as modified by AS/NZS 3003 for patient areas; and for equipment testing AS/NZS 3551.
2. What is a Body Protected Area (BPA)
A BPA is defined as an area where mains-powered electrical medical equipment is used on a patient (diagnosis, treatment, monitoring). This requires enhanced electrical protection (beyond normal wiring) because patients are more vulnerable.
Key features:
The electrical installation in the area must comply with AS/NZS 3003.
Use of medical-grade RCDs (10 mA trip) for socket outlets serving the area.
Signage: The area must be designated with a “Body Protected Area” sign (typically green) including date of last inspection.
All equipment (both medical and general appliances within the BPA) must be tested to medical-electrical equipment standard (AS/NZS 3551) or appropriate equivalent.
3. What the inspection by the inspector should cover
When performing the inspection/verfication the inspector should:
Visual & labelling/marking checks
Confirm that the room/area is clearly designated as a BPA, signage in place with last test/inspection date.
Check that all socket outlets in the area are protected by 10 mA RCDs (medical-grade) and that the RCDs are located within the area served (not elsewhere).
Ensure at least one outlet for cleaning equipment is provided and labelled (“Cleaning Purposes Only”) and is within or adjacent to the area per standard.
Check condition of wiring, outlets, switches, that nothing obviously unsafe or non-compliant.
Testing of protective devices and circuit behavior
Test RCD trip times/currents: For medical-grade RCDs (10 mA) ensure trip current/time meets standard.
Verify earthing/grounding / equipotential bonding as required (especially if BPA has additional protection requirements).
Confirm that circuits supplying the BPA are segregated / clearly identified from general circuits as needed.
Equipment testing / appliance checks
Confirm that all medical electrical equipment in the area (and general equipment that may touch or be used near a patient) is tagged/tested in accordance with AS/NZS 3551.
Check that the documentation (service records, calibration, tagging) for the equipment is available.
Documentation / certification
Provide a certificate or statement of verification that the BPA meets the requirements of AS/NZS 3003 (and relevant installation standard) following inspection.
The verification should include: date, inspector name, scope of work, results of tests, any remedial actions required.
The inspection cycle: the BPA should be inspected and re-verified at least every 12 months (unless local policy or standard specifies otherwise) as part of ongoing compliance.
Recommendations / remedial action
If any non-compliances are found (RCD not correct, signage missing, equipment not tested, etc), the inspector must document them and recommend corrective action, with timelines.
Follow up to ensure that the area remains safe for patient use until full compliance is achieved.
4. Who is responsible / when to inspect
The owner/operator of the facility (PCBU) must ensure that the BPA is safe and maintained. The inspector is independent of the installation work (i.e., cannot inspect work they carried out).
Inspection is required for new installations / alterations, and periodic verification for in-service.
Even if the standard AS/NZS 3003 is not mandated, it is recognised as a tool for compliance under the Health and Safety at Work Act. (Link to nzihe.org.nz)
Accident and emergency wards.
Allied health care providers, e.g. chiropractic, physiotherapy, optometry and naturopathic.
Anaesthetic bays.
Audiometry rooms.
Blood collection areas.
Day procedure theatres.
Delivery suites.
Dental surgeries.
Dermatology rooms.
Doctors consulting rooms.
Endoscopy theatres and procedure rooms.
General medical and surgical wards.
High dependency wards.
Imaging rooms.
Nurseries.
Operating theatres intended for non-cardiac surgery.
Patient examination rooms for outpatients.
Plasmapherisis areas.
Plaster rooms.
Recovery areas or wards associated with operating theatres and imaging rooms.
Respiratory function laboratories.
Resuscitation bays.
Stress test rooms.
Treatment rooms.
Ultrasound rooms.
Ensuites, bathrooms, shower rooms and toilets intended for patient use shall be wired as body-protected electrical areas.
The following Areas are deemed to be Body Protected Areas:
as per AS/NZS 3003
Contact Us
hreinspections@gmail.com
022 108 5729
Heinrich Oberholzer
Director