← Back to catalogue

J23263-75

EUDAMED

Class III (EU MDR)

Ref J23263-75

by Foosin Medical Supplies Inc., Ltd.

Identity

Model / Reference
J23263-75 EUDAMED

Identifiers

Primary DI / UDI-DI
06942339398196 EUDAMED
Basic UDI-DI
B-06942339398196 EUDAMED
EMDN Code
H010101020201,H010101020202 EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Greece 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

J23263-75 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000006957
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED edcbbb7e-a0b0-491a-94e8-c43152f66f9e 61 fields · synced Jul 9, 2026