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Sling - Amputee clip in situ
EUDAMEDFDA UDIClass I (EU MDR)
Ref MAA2050M-LLModel KKX522900L
Identity
- Trade Name
- Sling - Amputee clip in situ EUDAMEDArjo Sling FDA UDI
- Generic Name
- Patient lifting system amputee sling FDA UDI
- Device Name
- SLING - STANDING EUDAMEDAmputee clip in situ sling - LL FDA UDI
- Model / Reference
- KKX522900L EUDAMEDMAA2050M-LL EUDAMEDFDA UDI
- Description
- Amputee clip in situ sling - LL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05056097360119 EUDAMEDFDA UDI
- Basic UDI-DI
- 5060693520150VT EUDAMED
- FDA Product Code
- FSA FDA UDI
- EMDN Code
- V0805038002 NON-RIGID SUPPORTS FOR LIFTS (HARNESSES) EUDAMED
- GMDN Term
- Patient lifting system amputee sling FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 880.5510 FDA UDI
- Market of Registration
- Austria 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
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Sling - Amputee clip in situ by Arjohuntleigh AB — 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 | 5060693520150VT | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- ArjoHuntleigh AB
- EUDAMED SRN
- SE-MF-000000696
Sources (2)
- EUDAMED 8bcd611a-9a30-4e1a-bc28-8070740085ac 61 fields · synced Jul 14, 2026
- FDA UDI b5b01c61-2bc9-4eef-9b2c-f86393803b17 33 fields · synced May 30, 2026