Artificial Chamber Interface Z8 Liquid (AAC)
by SIE AG, Surgical Instrument Engineering
Ref 510.410.005Model Artificial Anterior Chamber (AAC) Product Range
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 | Number764016775AACXXXDP 07640167750535 | Date11 Jun 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- Withdrawn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
- Artificial Anterior Chamber (AAC)
- Model / Reference
- Artificial Anterior Chamber (AAC) Product Range, 510.410.005
- Primary DI / UDI-DI
- 07640167750535
- Basic UDI-DI
- 764016775AACXXXDP
- EMDN Code
- L170401 Corneal trephines, reusable
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CH-MF-000025018
- Authorised representative
- Ziemer Ophthalmology (DE) GmbH DE-AR-000005638
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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