plusoptiX A12R
Ref A12RModel A12C, A12R, S12C, S12R
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number04260184513116 | Date20 Oct 2022 | StatusListed |
| European Union | CE/MDR EUDAMED | Number426018451x12HA 04260184513116 | Date12 Apr 2022 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- plusoptiX A12R EUDAMEDplusoptiX 12 GUDID
- Generic Name
- External ocular measurement camera
- Model / Ref / Catalog
- A12C, A12R, S12C, S12R
- Primary DI / UDI-DI
- 04260184513116
- Basic UDI-DI
- 426018451x12HA
- Direct Marketing DI
- 04260184513116
- FDA Product Code
- HKO
- EMDN Code
- Q0299 Ophthalmic devices - other
- GMDN Term
- External ocular measurement camera
- Device Class
- Class I
- Regulation Number
- 886.1760
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Manufacturer details
- EUDAMED SRN
- DE-MF-000006138
Other devices from Plusoptix GmbH
Properties
Other properties (21)
- Sterile: No
- Single Use: 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
- Incorporates Medicinal Product: No
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Lot / Batch Number: No
- Expiration Date: No
- Manufacturing Date: No