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AK-Bipolar

EUDAMED

Class III (EU MDR)

Ref 1220-3822Model 38/22

by Beijing AK Medical Co., Ltd.

Identity

Trade Name
AK-Bipolar EUDAMED
Device Name
AK-Bipolar EUDAMED
Model / Reference
38/22 EUDAMED
1220-3822 EUDAMED

Identifiers

Primary DI / UDI-DI
06943735115011 EUDAMED
Basic UDI-DI
B-06943735115011 EUDAMED
EMDN Code
P090804050102 METAL FEMORAL HEADS, PARTIAL HIP REPLACEMENT 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

Category: Metallic femoral head prosthesis

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

Similar devices

Also classified as Metallic femoral head prosthesis.

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 48963156-9e9d-4444-b3c5-194f1a60449e 61 fields · synced Jul 10, 2026