Supine Headrest
by Libertech Corporation 3 variants
Ref AP112-UFG
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 | Number880923879LBT001LM 08809238796721 | Date27 Sep 2023 | 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- Withdrawn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
- Operation Room Gel Positioning Pad
- Model / Reference
- AP112-UFG
- Primary DI / UDI-DI
- 08809238796721
- Basic UDI-DI
- 880923879LBT001LM
- EMDN Code
- Z12011299 Patient positioning instruments – other
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- KR-MF-000024126
- Authorised representative
- CERT3GLOBAL, UNIPESSOAL, LDA. PT-AR-000037982
Other devices from Libertech Corporation
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