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Augment R-MOD
EUDAMEDClass IIb (EU MDR)
Ref BO76.2979.000.00Model Augment D.62 +18 mm Trabecular
Identity
- Device Name
- Augment R-MOD EUDAMED
- Model / Reference
- Augment D.62 +18 mm Trabecular EUDAMEDBO76.2979.000.00 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08050391090977 EUDAMED
- Basic UDI-DI
- B-08050391090977 EUDAMED
- Direct Marketing DI
- 08050391090977 EUDAMED
- EMDN Code
- P09088099 HIP PROSTHESES - OTHER ACCESSORIES EUDAMED
Classification
- Device Class
- Class IIb EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
Yes
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
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
Augment R-MOD by Lincotek Bologna S.r.l — 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-08050391090977 | Class IIb | Active |
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Manufacturer
- Manufacturer
- Lincotek Bologna S.r.l
- EUDAMED SRN
- IT-MF-000033944
Sources (1)
- EUDAMED 73f4fe95-afbf-4ee7-9259-93bcbe6b3d0e 61 fields · synced Jun 19, 2026