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Va-Lcp
EUDAMEDClass IIa (EU MDR)
Ref 03.133.386Model USFS 3D Templates
by Synthes GmbH
Identity
- Trade Name
- VA-LCP EUDAMED
- Device Name
- USFS 3D Templates EUDAMED
- Model / Reference
- USFS 3D Templates EUDAMED03.133.386 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07612334149336 EUDAMED
- Basic UDI-DI
- 7611819a00067JG EUDAMED
- Direct Marketing DI
- 07612334149336 EUDAMED
- EMDN Code
- Z12139099 VARIOUS ORTHOPAEDIC AND TRAUMATOLOGY INSTRUMENTS - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Belgium EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
Yes
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Category: Orthopaedic guidewire, reusable
The VA-LCP medical device, manufactured by Synthes GmbH, is a Class IIa implantable device used for the treatment of certain conditions. It has undergone rigorous professional testing and evaluation to ensure its safety and efficacy. This device is designed for use in various applications, including surgical implants.
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Also classified as Orthopaedic guidewire, reusable.
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Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 7611819a00067JG | Class IIa | Active |
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Manufacturer
- Manufacturer
- Synthes GmbH
- EUDAMED SRN
- CH-MF-000013345
- Authorised Representative
- DePuy Ireland UC IE-AR-000009328
Sources (1)
- EUDAMED 7f18e771-ddf3-4e65-9a5c-bec8bd1667e7 61 fields · synced Jul 19, 2026