Patient Sling
by Unitrend Co., Ltd. 12 variants
Ref SA6391500Model Patient Sling
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 | Number471988232PTSL0001BW 04719882320019 | Date4 Apr 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- Withdrawn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
- Patient Sling
- Model / Reference
- Patient Sling, SA6391500
- Primary DI / UDI-DI
- 04719882320019
- Basic UDI-DI
- 471988232PTSL0001BW
- Direct Marketing DI
- 04719882320019
- EMDN Code
- V0805038002 Non-rigid supports for lifts (harnesses)
- Device Class
- Class I
- Market of Registration
- Germany
Manufacturer details
- EUDAMED SRN
- TW-MF-000012250
- Authorised representative
- KOMAS Medical Technology GmbH DE-AR-000045617
Other devices from Unitrend Co., Ltd.
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