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K33163-75

EUDAMED

Class III (EU MDR)

Ref K33163-75 Model K33163-75

by Foosin Medical Supplies Inc., Ltd.

Identity

Model / Reference
K33163-75 EUDAMED

Identifiers

Primary DI / UDI-DI
06941813624165 EUDAMED
Basic UDI-DI
B-06941813624165 EUDAMED
EMDN Code
H010101020101,H010101020102 EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
France 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

K33163-75 by Foosin Medical Supplies Inc., 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-000006957
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 0c7e0266-acee-443b-b3f4-fbd9e6e718cf 61 fields · synced Jul 31, 2026