Maxi Move
by ArjoHuntleigh AB 2 variants
Ref KMCSUN-DModel KHA1010
Withdrawn
CE MDR, withdrawn
Ended
Withdrawn
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number5060693520082W3 05055982766951 | Date9 Jul 2024 | StatusWithdrawn |
| United States | GUDID listing GUDID | Number05055982766951 | Date29 Jul 2022 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic Name
- Mobile patient lifting system, electrically-powered
- Device Name
- Tenor
- Model / Reference
- KHA1010, KMCSUN-D
- Primary DI / UDI-DI
- 05055982766951
- Basic UDI-DI
- 5060693520082W3
- FDA Product Code
- FSA
- EMDN Code
- V0805030102 Electric mobile lifts
- GMDN Term
- Mobile patient lifting system, electrically-powered
- Device Class
- Class I
- Regulation Number
- 880.5510
- Market of Registration
- Austria
- GUDID distribution status
- Not in Commercial Distribution
Manufacturer details
- EUDAMED SRN
- SE-MF-000000696
Other devices from Arjohuntleigh AB
Properties
Other properties (19)
- Sterile: No
- Single Use: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Incorporates Medicinal Product: No
- Prescription Use: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Lot / Batch Number: No
- Expiration Date: No