Identity
- Trade Name
- Arjo Sling FDA UDI
- Generic Name
- General-purpose patient lifting system sling/harness FDA UDI
- Device Name
- Loop repositioning sling FDA UDI
- Model / Reference
- MAA6000 FDA UDI
- Description
- Loop repositioning sling FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05055982788298 FDA UDI
- FDA Product Code
- FSA FDA UDI
- GMDN Term
- General-purpose patient lifting system sling/harness FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5510 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Category: General-purpose patient lifting system sling/harness
Arjo Sling by Arjohuntleigh, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as General-purpose patient lifting system sling/harness.
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Arjohuntleigh, Inc.
Sources (2)
- FDA UDI b3dc8e3c-8923-484d-8e7e-18f63826089d 33 fields · synced Jun 20, 2026
- EUDAMED 1 fields · synced Jun 1, 2026