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K53193-75

EUDAMED

Class III (EU MDR)

Ref K53193-75Ref K33193-75 Model K33193-75

by Foosin Medical Supplies Inc., Ltd.

Identity

Model / Reference
K53193-75 EUDAMED
K33193-75 EUDAMED

Identifiers

Primary DI / UDI-DI
06941813624127 EUDAMED
06941813624172 EUDAMED
Basic UDI-DI
B-06941813624127 EUDAMED
B-06941813624172 EUDAMED
EMDN Code
H010101020102 POLYGLYCOLIC ACID MULTIFILAMENT WITH NEEDLE FOR VIDEO SURGERY EUDAMED
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

K53193-75 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 (2)

  • EUDAMED 81a72d39-440d-4722-aa1a-90dc00b89d9b 61 fields · synced Oct 6, 2026
  • EUDAMED 86df4035-bd4b-42f4-a0ef-4f6dc23f3c5d 61 fields · synced Aug 3, 2026