← Back to catalogue
B-Lo-Raiser
EUDAMEDFDA UDIClass I (EU MDR)
Ref B-LO-RAISERModel B-SSPUL-S
by GBUK Group
Identity
- Trade Name
- Banana FDA UDI
- Generic Name
- Solid-seat mobile patient lifting system seat FDA UDI
- Device Name
- Banana, Manual Raising Device, Lo-Raiser, Reusable FDA UDI
- Model / Reference
- B-SSPUL-S EUDAMEDB-LO-RAISER EUDAMEDFDA UDI
- Description
- Banana, Manual Raising Device, Lo-Raiser, Reusable FDA UDI
Identifiers
- Catalog Number
- B-Lo-Raiser FDA UDI
- Primary DI / UDI-DI
- 05060405746007 EUDAMEDFDA UDI
- Basic UDI-DI
- 506040574SlingsZB EUDAMED
- FDA Product Code
- IKX FDA UDI
- EMDN Code
- V0805038002 NON-RIGID SUPPORTS FOR LIFTS (HARNESSES) EUDAMED
- GMDN Term
- Solid-seat mobile patient lifting system seat FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 890.5050 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
B-Lo-Raiser by GBUK Group — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 506040574SlingsZB | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- GBUK Group
- EUDAMED SRN
- GB-MF-000002238
- Authorised Representative
- Qualrep Services B.V. NL-AR-000000537
Sources (2)
- EUDAMED 2a56d607-5ad4-4759-9d73-83ae768f8bce 61 fields · synced Jul 15, 2026
- FDA UDI 6c3b4182-dc63-4558-8f76-1844d1268dca 34 fields · synced May 30, 2026