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Ab1502h-75

EUDAMED

Class III (EU MDR)

Ref AB1502H-75

by Foosin Medical Supplies Inc., Ltd.

Identity

Model / Reference
AB1502H-75 EUDAMED

Identifiers

Primary DI / UDI-DI
06941813683049 EUDAMED
Basic UDI-DI
B-06941813683049 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

Ab1502h-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 9427e65c-64ac-4c02-ac5f-bec7ce3e1f38 61 fields · synced Jul 24, 2026