Tyrx™
Ref CMEZ6122INT
Tyrx™ (CMEZ6122INT) is a Class III device made by Medtronic, Inc., registered in EUDAMED on 5 Oct 2026 (Basic UDI-DI 0763000B000082688) with CE/MDR certificate MDR 773917 valid until 5 Sep 2029, active as of 24 Oct 2026.
Active
CE MDR
Valid until
5 Sep 2029
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberMDR 773917 | Date19 Oct 2026 | StatusActive |
Official records
- EUDAMED public site 0763000B000082688
Certificates
- MDR 773917 Active
Technical documentation EU MDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 19 Oct 2026
- Expires
- 5 Sep 2029
- Reason
- Change approved
- MDR 773917 Active
Technical documentation EU MDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 29 Jul 2026
- Expires
- 5 Sep 2029
- Reason
- Other
Timeline
- Registered EUDAMED 0763000B000082688
- Certificate issued EUDAMED MDR 773917
- Certificate expires EUDAMED MDR 773917
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Absorbable Antibacterial Envelope
- Model / reference
- CMEZ6122INT
- Primary DI / UDI-DI
- 00763000534615
- Basic UDI-DI
- 0763000B000082688
- EMDN code
- P900201 Polyglycolic acid and associations meshes
- Device class
- Class III
- EU registration type
- Standard device
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- US-MF-000023316
- Authorised representative
- Medtronic B.V. NL-AR-000006050
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