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Simpass

EUDAMED

Class IIa (EU MDR)

Ref SND50060-150Model Simpass Endo18

by Simeks Tibbi Urunler San. ve Tic LTD STI

Identity

Trade Name
Simpass EUDAMED
Device Name
Simpass Endo18 OTW PTA Balloon Dilatation Catheter EUDAMED
Model / Reference
Simpass Endo18 EUDAMED
SND50060-150 EUDAMED

Identifiers

Primary DI / UDI-DI
08699343625081 EUDAMED
Basic UDI-DI
86993436PTA18OTWHK EUDAMED
EMDN Code
C010402020101 PTA BALLOON DILATATION CATHETERS 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

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: Peripheral angioplasty balloon catheter, basic

Simpass by Simeks Tibbi Urunler San. ve Tic LTD STI — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral angioplasty balloon catheter, basic.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
TR-MF-000015871

Sources (1)

  • EUDAMED d20242e8-366c-4846-a7f2-57cb22d537ec 61 fields · synced Jun 19, 2026