Multigen Plus Knee - Cocrmo+poroti Tibial Plate #0 - Mobile Uncemented
Ref 6623.10.005Model 80333903K013E2
Active
CE MDR
Valid until
10 Sep 2029
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number80333903K013E2 08033390014915 | Date10 Aug 2026 | StatusActive |
Certificates
- 053-00-02-MDR Active
Technical documentation EU MDR
- Certifier
- ITALCERT SRL 0426
- Issued
- 14 Oct 2025
- Expires
- 10 Sep 2029
- Reason
- Add device or group
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
- Austria
- Belgium
- Bulgaria
- Croatia
- Cyprus
- Czechia
- Denmark
- Estonia
- Finland
- France
- Germany
- Greece
- Hungary
- Iceland
- Ireland
- Italy
- Latvia
- Liechtenstein
- Lithuania
- Luxembourg
- Malta
- Netherlands
- Northern Ireland
- Norway
- Poland
- Portugal
- Romania
- Slovakia
- Slovenia
- Spain
- Sweden
- Türkiye
Specification
- Model / Reference
- 80333903K013E2, 6623.10.005
- Primary DI / UDI-DI
- 08033390014915
- Basic UDI-DI
- 80333903K013E2
- EMDN Code
- P090903020102 Bicompartmental primary implant uncemented mobile bearing tibial plates
- Device Class
- Class III
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- IT-MF-000010690
Other devices from LIMACORPORATE S.p.A.
Properties
Other properties (10)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No