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Alvision

EUDAMED

Class III (EU MDR)

Ref 501110188608

by Alvimedica Tibbi Urunler San. ve Dis Tic. A.S.

Identity

Trade Name
Alvision EUDAMED
Device Name
Alvision Interventional Cardiology Diagnostic Catheter EUDAMED
Model / Reference
501110188608 EUDAMED

Identifiers

Primary DI / UDI-DI
08699195528219 EUDAMED
Basic UDI-DI
086991955Alvision5D EUDAMED
Direct Marketing DI
08699195528219 EUDAMED
EMDN Code
C0104010101 CARDIAC ANGIOGRAPHY DIAGNOSTIC CATHETERS EUDAMED

Classification

Device Class
Class III 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: Angiographic catheter, single-use

Alvision by Alvimedica Tibbi Urunler San. ve Dis Tic. A.S. — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Angiographic catheter, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
TR-MF-000029915

Sources (1)

  • EUDAMED 460c4d38-c665-418f-877e-999e79e9ff62 61 fields · synced Jun 20, 2026