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P41183-75

EUDAMED

Class IIb (EU MDR)

Ref P41183-75Model POLYPROPYLENE

by Foosin Medical Supplies Inc., Ltd.

Identity

Model / Reference
POLYPROPYLENE EUDAMED
P41183-75 EUDAMED

Identifiers

Primary DI / UDI-DI
06941813678885 EUDAMED
Basic UDI-DI
69418136NA-suturesIIbP7V EUDAMED
Direct Marketing DI
06941813678885 EUDAMED
EMDN Code
H010201010401,H010201010402 EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Romania EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

Yes

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Polyolefin/fluoropolymer suture, monofilament

P41183-75 by Foosin Medical Supplies Inc., Ltd. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Polyolefin/fluoropolymer suture, monofilament.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000006957
Authorised Representative
MedNet EC-REP C III GmbH DE-AR-000011196

Sources (1)

  • EUDAMED 8036fe69-0fea-4322-a18c-86f0db9a1d45 61 fields · synced Sep 17, 2026