Identity
- Trade Name
- GENDRON FDA UDI
- Generic Name
- Mobile patient lifting system, electrically-powered FDA UDI
- Device Name
- PATIENT LIFT 700LB CAPACITY FDA UDI
- Model / Reference
- PL700 FDA UDI
- Description
- PATIENT LIFT 700LB CAPACITY FDA UDI
Identifiers
- Primary DI / UDI-DI
- M368PL7001 FDA UDI
- FDA Product Code
- FNG FDA UDI
- GMDN Term
- Mobile patient lifting system, electrically-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Mobile patient lifting system, electrically-powered
Gendron by GF Health Products, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Mobile patient lifting system, electrically-powered.
- EZ Way — EZ Way, Inc. · Class I
- BestStand — BESTCARE, L.L.C. · Class I
- Maxi Sky 2 — Arjohuntleigh, Inc. · Class I
- Maxi Sky 2 — Arjohuntleigh, Inc. · Class I
- Maxi Move — Arjohuntleigh, Inc. · Class I
- EZ Way — EZ Way, Inc. · Class I
- Maxi 500 — Arjohuntleigh, Inc. · Class I
- EZ Smart Stand — EZ Way, Inc. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- GF Health Products, Inc
Sources (1)
- FDA UDI 025eb1d2-d043-48f5-a2f9-bdcd99cef72f 34 fields · synced Jun 8, 2026