05993022299239
by Medicontur Medical Engineering Ltd.
Part of a family of 400 devices: see the family page
Ref 05993022299239Model 677CTA
05993022299239 is a Class IIb device made by Medicontur Medical Engineering Ltd., registered in EUDAMED on 2 Jun 2026 (Basic UDI-DI 599302677CTARP) with CE/MDR certificate 2023-MDR/QS-048/A valid until 10 Nov 2028, active as of 23 Oct 2026.
Active
CE MDR
Valid until
10 Nov 2028
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number599302677CTARP 05993022299239 | Date2 Jun 2026 | StatusActive |
Official records
- EUDAMED public site 599302677CTARP
Certificates
- 2023-MDR/QS-048/A Active
Quality management system EU MDR
- Certifier
- 3EC International a.s. 2265
- Issued
- 12 Dec 2024
- Expires
- 10 Nov 2028
- Reason
- Other
- 2023-MDR/TD-048/A Active
Technical documentation EU MDR
- Certifier
- 3EC International a.s. 2265
- Issued
- 12 Dec 2024
- Expires
- 10 Nov 2028
- Reason
- Other
Timeline
- Certificate issued EUDAMED 2023-MDR/QS-048/A
- Certificate issued EUDAMED 2023-MDR/TD-048/A
- Registered EUDAMED 599302677CTARP
- Certificate expires EUDAMED 2023-MDR/QS-048/A
- Certificate expires EUDAMED 2023-MDR/TD-048/A
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / reference
- 677CTA, 05993022299239
- Primary DI / UDI-DI
- 05993022299239
- Basic UDI-DI
- 599302677CTARP
- EMDN code
- P030102090302 IOLs, APHAKIC, MONOFOCAL, TORIC, HYDROPHILIC ACRYLIC
- Device class
- Class IIb
- EU registration type
- Standard device
- EU market of registration
- Hungary
Manufacturer details
- EUDAMED SRN
- HU-MF-000024195
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