05993022927552
by Medicontur Medical Engineering Ltd.
Part of a family of 324 devices: see the family page
Ref 05993022927552Model 860PETY
05993022927552 is a Class IIb device made by Medicontur Medical Engineering Ltd., registered in EUDAMED on 21 May 2026 (Basic UDI-DI 599302860PETYNW) with CE/MDR certificate 2023-MDR/QS-046/B 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 | Number2023-MDR/QS-046/B | Date11 Sep 2026 | StatusActive |
Official records
- EUDAMED public site 599302860PETYNW
Certificates
- 2023-MDR/QS-046/B Active
Quality management system EU MDR
- Certifier
- 3EC International a.s. 2265
- Issued
- 11 Sep 2026
- Expires
- 10 Nov 2028
- Reason
- Other
- 2023-MDR/TD-046/B Active
Technical documentation EU MDR
- Certifier
- 3EC International a.s. 2265
- Issued
- 11 Sep 2026
- Expires
- 10 Nov 2028
- Reason
- Other
Timeline
- Registered EUDAMED 599302860PETYNW
- Certificate issued EUDAMED 2023-MDR/QS-046/B
- Certificate issued EUDAMED 2023-MDR/TD-046/B
- Certificate expires EUDAMED 2023-MDR/QS-046/B
- Certificate expires EUDAMED 2023-MDR/TD-046/B
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / reference
- 860PETY, 05993022927552
- Primary DI / UDI-DI
- 05993022927552
- Basic UDI-DI
- 599302860PETYNW
- EMDN code
- P030102090301 IOLs, APHAKIC, MONOFOCAL, TORIC, HYDROPHOBIC 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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