← Back to catalogue
Titanium Trabecular Augment (GPS-I)
EUDAMEDClass IIb (EU MDR)
Ref A2505-5201Model 52L
Identity
- Trade Name
- Titanium Trabecular Augment (GPS-I) EUDAMED
- Device Name
- Titanium Trabecular Augment (GPS-I) EUDAMED
- Model / Reference
- 52L EUDAMEDA2505-5201 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06943735154195 EUDAMED
- Basic UDI-DI
- B-06943735154195 EUDAMED
- EMDN Code
- P09088003 HIP PROSTHESES AUGMENTS EUDAMED
Classification
- Device Class
- Class IIb EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
Yes
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Titanium Trabecular Augment (GPS-I) by Beijing AK Medical Co., Ltd. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-06943735154195 | Class IIb | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Beijing AK Medical Co., Ltd.
- EUDAMED SRN
- CN-MF-000018814
- Authorised Representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Sources (1)
- EUDAMED dff12ec7-823e-4a7d-acdf-e10f1c230210 61 fields · synced Oct 6, 2026