Electric patient lifter
by Pukang Health Industry (Chongqing) Co., Ltd.
Ref FS-10Model FS-10、FS-11、FS-12、FS-13、FS-14、FS-15、FS-21、FS-22、FS-23、FS-24、FS-25
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 | Number697897482patientlifterAN 06978974822956 | Date13 Mar 2026 | 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- Withdrawn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
- Electric patient lifter
- Model / Reference
- FS-10、FS-11、FS-12、FS-13、FS-14、FS-15、FS-21、FS-22、FS-23、FS-24、FS-25, FS-10
- Primary DI / UDI-DI
- 06978974822956
- Basic UDI-DI
- 697897482patientlifterAN
- EMDN Code
- V0805030101 Manual mobile lifts
- Device Class
- Class I
- Market of Registration
- Austria
Manufacturer details
- EUDAMED SRN
- CN-MF-000051929
- Authorised representative
- SUNGO Europe B.V. NL-AR-000000247
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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