Our re-certification process
Every device we sell is brought back to manufacturer specification by our experienced biomedical technicians — then certified and warrantied before it ships.
“Re-certified” isn’t a marketing term for us — it’s a documented, four-stage process performed by trained biomedical technicians and backed by our ISO 9001:2015 registration and DOTmed certification. Here is exactly what happens to every unit before it reaches your facility.
1. Source & intake
Units are sourced from trusted hospitals, clinics and OEMs, then logged, photographed and visually inspected on arrival. Each device is matched to its model history and service records so we know precisely what we’re working with.
2. Repair & replace
Worn or failing components are repaired or replaced with OEM-grade parts. Batteries are renewed, internal cleaning is performed, and any safety-relevant parts are brought to current spec. Nothing ships with a known defect.
3. Calibrate & test
Each unit is calibrated and put through full functional and electrical-safety testing to the manufacturer’s specification, using traceable test equipment. Performance is verified end-to-end — not just powered on.
4. Certify & ship
A certificate of conformance is issued, the unit is covered by our 12-month parts-and-labor warranty, and it’s packed and shipped insured nationwide. You receive documentation you can hand straight to your biomed department.
Credentials
Precision MedLab is ISO 9001:2015 registered (Biomedical Equipment Services) and DOTmed certified, with current biomed training on platforms including Hillrom CVSM, Philips IntelliVue and ZOLL R Series.