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Titanium Trabecular Augment

EUDAMED

Class III (EU MDR)

Ref 5001-5848Model 58/48

by Beijing AK Medical Co., Ltd.

Identity

Trade Name
Titanium Trabecular Augment EUDAMED
Device Name
Titanium Trabecular Augment EUDAMED
Model / Reference
58/48 EUDAMED
5001-5848 EUDAMED

Identifiers

Primary DI / UDI-DI
06943735150036 EUDAMED
Basic UDI-DI
B-06943735150036 EUDAMED
EMDN Code
P09088003 HIP PROSTHESES AUGMENTS EUDAMED

Classification

Device Class
Class III 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 by Beijing AK Medical Co., Ltd. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000018814
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 38a37de8-2ddd-4d94-928b-3bb972834e80 61 fields · synced Sep 18, 2026