Lcp
by Synthes GmbH 1,000+ variants
Ref 241.441SModel LCP Distal Tibial Plate anterolateral, Stainless Steel
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number7611819a00485K6 07611819838772 | Date21 May 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- LCP Distal Tibial Plate anterolateral, Stainless Steel
- Model / reference
- LCP Distal Tibial Plate anterolateral, Stainless Steel, 241.441S
- Primary DI / UDI-DI
- 07611819838772
- Basic UDI-DI
- 7611819a00485K6
- EMDN code
- P09120501 Osteosynthesis compression plates
- Device class
- Class IIb
- EU registration type
- Standard device
- EU market of registration
- Belgium
Manufacturer details
- EUDAMED SRN
- CH-MF-000013345
- Authorised representative
- DePuy Ireland UC IE-AR-000009328
Other devices from Synthes GmbH
Properties
Other properties (11)
- Sterilise before use: No
- Reusable: No
- Contains latex: No
- Reprocessed single-use device: No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No