← Back to catalogue
HM Repositioning/Supine Sling 3498
EUDAMEDFDA UDIClass I (EU MDR)
Ref 3498 00000001
Identity
- Trade Name
- HM Repositioning/Supine Sling 3498 EUDAMEDHandi-Move Sling FDA UDI
- Generic Name
- Patient lifting system stretcher FDA UDI
- Device Name
- Spreaderbar + Sling EUDAMEDRepositioning/Supine Sling 3498 FDA UDI
- Model / Reference
- 3498 00000001 EUDAMEDFDA UDI
- Description
- Repositioning/Supine Sling 3498 FDA UDI
Identifiers
- Catalog Number
- 3498 00000001 FDA UDI
- Primary DI / UDI-DI
- 05404016612069 EUDAMEDFDA UDI
- Basic UDI-DI
- 54040166NRBSK5 EUDAMED
- FDA Product Code
- FSA FDA UDI
- EMDN Code
- V0805038002 NON-RIGID SUPPORTS FOR LIFTS (HARNESSES) EUDAMED
- GMDN Term
- Patient lifting system stretcher FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 880.5510 FDA UDI
- Market of Registration
- Belgium 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
HM Repositioning/Supine Sling 3498 by Handi-Move NV — 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 | 54040166NRBSK5 | 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
- Handi-Move NV
- EUDAMED SRN
- BE-MF-000016949
Sources (2)
- EUDAMED 4a4e84c8-a723-46ca-978e-358f94f2fa36 61 fields · synced Jul 18, 2026
- FDA UDI dfd4cee4-e2dd-49fe-b067-b880aab71163 35 fields · synced May 30, 2026