Identity
- Trade Name
- Raizer FDA UDI
- Generic Name
- Patient fall-recovery chair, manual FDA UDI
- Device Name
- A manually operated device to lift a person from the floor into a seated position. FDA UDI
- Model / Reference
- M FDA UDI
- Description
- A manually operated device to lift a person from the floor into a seated position. FDA UDI
Identifiers
- Catalog Number
- 105040 FDA UDI
- Primary DI / UDI-DI
- 05060572010352 FDA UDI
- FDA Product Code
- FSA FDA UDI
- GMDN Term
- Patient fall-recovery chair, manual 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Patient fall-recovery chair, manual
Raizer by The Kirton Healthcare Group Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- The Kirton Healthcare Group Limited
Sources (1)
- FDA UDI dc9cda55-a616-4fa7-93c8-0b0eb1289adf 34 fields · synced May 30, 2026