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Ares

EUDAMED

Class IIa (EU MDR)

Ref ARES - GW2108

by Ares Medikal Sanayi Ticaret Ltd. Şti.

Identity

Trade Name
ARES EUDAMED
Device Name
Guide Wire EUDAMED
Model / Reference
ARES - GW2108 EUDAMED

Identifiers

Primary DI / UDI-DI
86989077499668 EUDAMED
Basic UDI-DI
B-86989077499668 EUDAMED
EMDN Code
C04020101 PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, HYDROPHILIC EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

Ares by Ares Medikal Sanayi Ticaret Ltd. Şti. — Class IIa — 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-000029015

Sources (1)

  • EUDAMED 4652422b-b88c-4930-85cd-29bba9b647e5 61 fields · synced Oct 6, 2026