← Back to catalogue
Handi Seat Sling PVC for Pools
EUDAMEDFDA UDIClass I (EU MDR)
Ref 3473 00000002
Identity
- Trade Name
- Handi Seat Sling PVC for Pools EUDAMEDHandi-Move Sling FDA UDI
- Generic Name
- General-purpose patient lifting system sling/harness FDA UDI
- Device Name
- Spreaderbar + Sling EUDAMEDHandi Seat Sling 3473 for Pools FDA UDI
- Model / Reference
- 3473 00000002 EUDAMEDFDA UDI
- Description
- Handi Seat Sling 3473 for Pools FDA UDI
Identifiers
- Catalog Number
- 3473 00000002 FDA UDI
- Primary DI / UDI-DI
- 05404016611574 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
- General-purpose patient lifting system sling/harness 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
Handi Seat Sling PVC for Pools 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 3685778c-6e2d-4d2b-99d8-37c627bf1262 61 fields · synced Jul 13, 2026
- FDA UDI 86dae5c6-5bdf-4db4-9bdc-add23ddaee16 35 fields · synced May 30, 2026