M-Series Fixed Patient Lifter
by Savaria Concord Lifts 56 variants
Ref M2F200-1003-02-EUModel M-Series
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number0688503FIXEDLIFTJE 10688503001327 | Date23 Apr 2025 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- M-Series Fixed Patient Lifter
- Model / Reference
- M-Series, M2F200-1003-02-EU
- Primary DI / UDI-DI
- 10688503001327
- Basic UDI-DI
- 0688503FIXEDLIFTJE
- EMDN Code
- V08050302 Electric fixed lifts
- Device Class
- Class I
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- CA-MF-000010883
- Authorised representative
- Advena SRL IT-AR-000051131
Other devices from Savaria Concord Lifts
Properties
Other properties (13)
- Sterile: 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
- Measuring Function: No
- Incorporates Medicinal Product: No