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Ares

EUDAMED

Class I (EU MDR)

Ref BID3020KPCTModel BID6000

by Ares Medikal Sanayi Ticaret Ltd. Şti.

Identity

Trade Name
ARES EUDAMED
Device Name
Balloon Inflation Device EUDAMED
Model / Reference
BID6000 EUDAMED
BID3020KPCT EUDAMED

Identifiers

Primary DI / UDI-DI
86989077505420 EUDAMED
Basic UDI-DI
B-86989077505420 EUDAMED
EMDN Code
C010402020101 PTA BALLOON DILATATION CATHETERS EUDAMED

Classification

Device Class
Class I 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 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 1c2af8ab-89b0-4bf5-8c09-247d107fb4e7 61 fields · synced Oct 5, 2026