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Knee prosthesis- femoral condyle

EUDAMED

Class III (EU MDR)

Ref 51401-7Model XR A302 / 4L

by Beijing LiDaKang Technology Co., Ltd.

Identity

Device Name
Knee prosthesis- femoral condyle EUDAMED
Model / Reference
XR A302 / 4L EUDAMED
51401-7 EUDAMED

Identifiers

Primary DI / UDI-DI
06942494979834 EUDAMED
Basic UDI-DI
B-06942494979834 EUDAMED
EMDN Code
P09090501 REVISION KNEE PROSTHESES FEMORAL COMPONENTS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye 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

Knee prosthesis- femoral condyle by Beijing LiDaKang Technology 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-000027201
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED a9e8ffe0-8048-4894-bb0b-9694060fd7a4 61 fields · synced Jun 19, 2026