Unity Total Knee System 1124302
by Corin Ltd
Ref 1124302Model Unity Total Knee System
Active
CE MDD
Valid until
Not listed
FDA recalls
None foundDocuments
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-05055343897911 05055343897911 | Date28 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number05055343897911 | Date6 Mar 2018 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Tibial Augment Screw 10mm EUDAMEDUnity Total Knee System GUDID
- Generic Name
- Orthopaedic bone screw, non-bioabsorbable, sterile
- Device Name
- Unity knee Femoral / Tibial Augment Screw
- Model / Ref / Catalog
- 1124302, Unity Total Knee System
- Primary DI / UDI-DI
- 05055343897911
- Basic UDI-DI
- B-05055343897911
- 510(k) Number
- FDA Product Code
- JWH
- EMDN Code
- P090999 Knee prostheses - other
- GMDN Term
- Orthopaedic bone screw, non-bioabsorbable, sterile
- Device Class
- Class IIb EUDAMEDClass II GUDID
- Regulation Number
- 888.3560
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Radiation Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIb | Class II |
| Implantable | Yes | No |
Other devices from Corin Ltd
Properties
Other properties (18)
- 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
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No