PCREE Explainer Video

What Is PCREE Testing? A Plain-Language Guide for SNFs

4 minutes. Everything your facility needs to know about CMS compliance, NFPA 99, and what a certified inspection looks like.

4:31  ·  Patient Care Related Electrical Equipment  ·  CMS 42 CFR 483.70  ·  NFPA 99 Chapter 10

Video Chapters

0:00Introduction — why this matters for CMS survey prep
0:20What does PCREE stand for?
0:45Federal mandate — CMS 42 CFR 483.70 & NFPA 99 Chapter 10
1:15What equipment gets tested? (hospital beds, IV pumps, Hoyer lifts & more)
1:30The 4-step PCREE inspection process
1:55How often is testing required? (annual + on admission)
2:15Consequences of non-compliance — F-tags, fines, Medicare risk
2:35Who should perform PCREE testing? (CBET credential explained)
2:50How to get a free quote at PCREEtest.com
Key takeaway: PCREE testing is federally required under CMS Conditions of Participation (42 CFR 483.70) and NFPA 99 Chapter 10. Every SNF must test all patient-care electrical devices at least annually — with device-level documentation a CMS surveyor can review on demand.

Frequently Asked Questions

PCREE stands for Patient Care Related Electrical Equipment — any electrically powered device used in the direct care of residents in a skilled nursing facility. The term is defined in NFPA 99 and enforced through CMS Life Safety Code surveys.
Yes. CMS Conditions of Participation 42 CFR 483.70(a) requires all SNFs to maintain safe and functional electrical equipment. NFPA 99 Chapter 10 provides the technical standard CMS references for testing intervals, pass/fail thresholds, and documentation. Failure to comply results in F-tag citations.
At a minimum, annually — once per calendar year for every PCREE device in the facility. Additionally, any device brought in by a new resident must be tested before being used in patient care. Re-testing is also required after any repair or device modification.
Hospital beds and controls, infusion and IV pumps, sequential compression devices, Hoyer and patient lifts, blood pressure monitors, heating pads and therapy units, and any other electrically powered device that provides therapy, monitoring, or mobility to residents. The rule: if it plugs in and touches a patient, it qualifies.
CMS can issue F-tag citations (specifically F925 under the Life Safety Code), civil money penalties starting at $100/day and escalating to $10,000+/day for repeat violations, and in the most serious cases a threat to your Medicare and Medicaid certification. Documentation from a credentialed technician is your primary defense during surveys.
A CBET (Certified Biomedical Equipment Technician) credentialed through AAMI is the industry standard. The technician must use a calibrated electrical safety analyzer (ESA) with a current NIST-traceable calibration certificate. Always ask for the technician's credential number and ESA calibration records before scheduling.

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