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Ab-150

EUDAMED

Class III (EU MDR)

Ref AB-150

by Foosin Medical Supplies Inc., Ltd.

Identity

Model / Reference
AB-150 EUDAMED

Identifiers

Primary DI / UDI-DI
06942339399896 EUDAMED
Basic UDI-DI
B-06942339399896 EUDAMED
EMDN Code
H010101020203 POLYGLYCOLIC WITH LACTIC ACID MULTIFILAMENT WITHOUT NEEDLE 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

Ab-150 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 d9c25654-22af-4b1f-9e24-07707e6dc105 61 fields · synced Jul 9, 2026