Identity
- Trade Name
- ResQUp FDA UDI
- Generic Name
- Mobile patient lifting system, manual FDA UDI
- Device Name
- Self-Recovery device to assist a fallen person moving themselves to a seated position after a non-injurious fall. Color: Midnight FDA UDI
- Model / Reference
- Midnight FDA UDI
- Description
- Self-Recovery device to assist a fallen person moving themselves to a seated position after a non-injurious fall. Color: Midnight FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860003643105 FDA UDI
- FDA Product Code
- IKX FDA UDI
- GMDN Term
- Mobile patient lifting system, manual FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5050 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
ResQUp by Safe Patient Solutions, L.L.C. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Safe Patient Solutions, L.L.C.
Sources (1)
- FDA UDI c5f597de-299b-4a25-a7bd-9207f8e5fbd4 33 fields · synced Jun 8, 2026