Identity
- Trade Name
- Vive FDA UDI
- Generic Name
- Mobile patient lifting system, manual FDA UDI
- Device Name
- Core Hydraulic Patient Lift FDA UDI
- Model / Reference
- MOB1120WHT FDA UDI
- Description
- Core Hydraulic Patient Lift FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810178880522 FDA UDI
- FDA Product Code
- FNG FDA UDI
- GMDN Term
- Mobile patient lifting system, manual 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
Yes
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Mobile patient lifting system, manual
Vive by Vive Health Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Mobile patient lifting system, manual.
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- Lumex — GF Health Products, Inc · Class I
- ResQUp — Safe Patient Solutions, L.L.C. · Class I
- BestLift — BESTCARE, L.L.C. · Class I
- SARA STEDY — Arjohuntleigh, Inc. · Class I
- Lumex — GF Health Products, Inc · Class I
- BestMove — BESTCARE, L.L.C. · 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 |
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Manufacturer
- Manufacturer
- Vive Health Llc
Sources (1)
- FDA UDI 2d798be8-c0c0-4e7a-92bd-2c8b99f4e6e7 33 fields · synced May 30, 2026