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Knee prosthesis -femoral condyle

EUDAMED

Class III (EU MDR)

Ref A5100-02RModel RY A203 / 2#R

by Beijing LiDaKang Technology Co., Ltd.

Identity

Device Name
Knee prosthesis -femoral condyle EUDAMED
Model / Reference
RY A203 / 2#R EUDAMED
A5100-02R EUDAMED

Identifiers

Primary DI / UDI-DI
06942494903471 EUDAMED
Basic UDI-DI
B-06942494903471 EUDAMED
EMDN Code
P0909030103 BICOMPARTMENTAL PRIMARY IMPLANT CEMENTABLE 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 b15783d3-887d-4c00-9026-ac7ffea6a781 61 fields · synced Oct 7, 2026