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Pedesente

EUDAMED

Class III (EU MDR)

Ref D233Model With or without needle(s)

by Doğsan Tibbi̇ Malzeme Sanayi̇ A.ş.

Identity

Trade Name
PEDESENTE EUDAMED
Device Name
PEDESENTE EUDAMED
Model / Reference
With or without needle(s) EUDAMED
D233 EUDAMED

Identifiers

Primary DI / UDI-DI
08698147931299 EUDAMED
Basic UDI-DI
8698147S100D0SZ EUDAMED
EMDN Code
H010101010101,H010101010102 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

Pedesente by Doğsan Tibbi̇ Malzeme Sanayi̇ A.ş. — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

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 40a3defe-1d1d-4110-ad97-9522b93ffca0 61 fields · synced Jun 20, 2026