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Ares

EUDAMED

Class I (EU MDR)

Ref ARES - M5000Model ARES - M5000 - Manifold

by Ares Medikal Sanayi Ticaret Ltd. Şti.

Identity

Trade Name
ARES EUDAMED
Device Name
Manifold EUDAMED
Model / Reference
ARES - M5000 - Manifold EUDAMED
ARES - M5000 EUDAMED

Identifiers

Primary DI / UDI-DI
86989077411066 EUDAMED
Basic UDI-DI
B-86989077411066 EUDAMED
EMDN Code
Z11030185 DIGITAL ANGIOGRAPHY SYSTEMS - CONSUMABLES EUDAMED

Classification

Device Class
Class I 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

Ares by Ares Medikal Sanayi Ticaret Ltd. Şti. — Class I — 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 89c95391-3db2-4664-9edd-8e751263c91c 61 fields · synced Oct 6, 2026