Zuit®
by Zuitlab, Lda. EUDAMED
Withdrawn
Ref ZUITHO30
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number5600208360OCULARXS | Date17 Dec 2024 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
European Union — CE/MDR Withdrawn
Certificates
No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.
Specification
- Device Name
- ZUIT® HipoOcular
- Model / Reference
- ZUITHO30
- Primary DI / UDI-DI
- 05600208360002
- Basic UDI-DI
- 5600208360OCULARXS
- EMDN Code
- V9099 Various devices not included in other classes - other
- Device Class
- Class I
- Market of Registration
- Portugal
Manufacturer details
- EUDAMED SRN
- PT-MF-000045541
Other devices from Zuitlab, Lda.
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