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Pegelak

EUDAMED

Class III (EU MDR)

Ref L103

by Doğsan Tibbi̇ Malzeme Sanayi̇ A.ş.

Identity

Trade Name
Pegelak EUDAMED
Device Name
Pegelak EUDAMED
Model / Reference
L103 EUDAMED

Identifiers

Primary DI / UDI-DI
08698147923775 EUDAMED
Basic UDI-DI
B-08698147923775 EUDAMED
EMDN Code
H010101020201,H010101020202 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

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

Pegelak by Doğsan Tibbi̇ Malzeme Sanayi̇ A.ş. — 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
TR-MF-000016026

Sources (1)

  • EUDAMED 0065abf3-5250-4c78-8338-feaa470bd587 61 fields · synced Jun 19, 2026