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Propilen

EUDAMED

Class III (EU MDR)

Ref P79056Model With or without needle(s)

by Doğsan Tibbi̇ Malzeme Sanayi̇ A.ş.

Identity

Trade Name
PROPILEN EUDAMED
Device Name
PROPILEN EUDAMED
Model / Reference
With or without needle(s) EUDAMED
P79056 EUDAMED

Identifiers

Primary DI / UDI-DI
08698147915879 EUDAMED
Basic UDI-DI
8698147S000P0TS EUDAMED
EMDN Code
H010201010401,H010201010402 EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

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

Propilen by Doğsan Tibbi̇ Malzeme Sanayi̇ A.ş. — Class III — 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
TR-MF-000016026

Sources (1)

  • EUDAMED 85fc0eb6-669a-4902-ab6f-2759b0ae0304 61 fields · synced Jun 19, 2026