← Back to catalogue
Sling - Clip bathing in situ sling – unpadded legs
EUDAMEDFDA UDIClass I (EU MDR)
Ref MAA2070M0XLModel KKX522900LRef MAA2070M-LL
Identity
- Trade Name
- Sling - Clip bathing in situ sling – unpadded legs EUDAMEDArjo Sling FDA UDI
- Generic Name
- General-purpose patient lifting system sling/harness FDA UDI
- Device Name
- SLING - STANDING EUDAMEDClip bathing in situ sling – unpadded legs -LL FDA UDI
- Model / Reference
- KKX522900L EUDAMEDMAA2070M0XL EUDAMEDMAA2070M-LL EUDAMEDFDA UDI
- Description
- Clip bathing in situ sling – unpadded legs -LL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05056341671077 EUDAMED05056097346809 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
- 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
- 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 - Clip bathing in situ sling – unpadded legs 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- ArjoHuntleigh AB
- EUDAMED SRN
- SE-MF-000000696
Sources (3)
- EUDAMED e3351dc1-c265-45e8-b349-a2fefa2cd284 61 fields · synced Jul 17, 2026
- EUDAMED abe83713-639c-4221-ab54-e883b4ee15af 61 fields · synced May 17, 2026
- FDA UDI ead530a0-672c-4d0b-8374-65e1fc2fa093 33 fields · synced May 29, 2026