Identity
- Trade Name
- Hydraulic Patient Lifter FDA UDI
- Generic Name
- Manual patient lifting belt/harness FDA UDI
- Model / Reference
- 10704 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00616784070414 FDA UDI
- FDA Product Code
- FSA FDA UDI
- GMDN Term
- Manual patient lifting belt/harness FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5510 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Mobile patient lifting system, manualManual patient lifting belt/harness
Hydraulic Patient Lifter by Dynarex Corp. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Dynarex Corp.
Sources (1)
- FDA UDI 312e6265-bf4d-4713-a378-e8cf8f1c6f3f 32 fields · synced Jun 8, 2026