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Disposet

EUDAMED

Class IIa (EU MDR)

Ref 959-511003-000

by Di̇sposet Tibbi̇ Ürünler Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

Identity

Trade Name
Disposet EUDAMED
Device Name
Aortic Punch EUDAMED
Model / Reference
959-511003-000 EUDAMED

Identifiers

Primary DI / UDI-DI
08681049566867 EUDAMED
Basic UDI-DI
B-08681049566867 EUDAMED
EMDN Code
C01901201 AORTIC PUNCHES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

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

Category: Aorta punch, single-use

Disposet by Di̇sposet Tibbi̇ Ürünler Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Aorta punch, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TR-MF-000018945

Sources (1)

  • EUDAMED 037ba1ba-1320-4a12-bf0a-f92b0d746f1f 61 fields · synced Jun 20, 2026