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Ares

by Ares Medikal Sanayi Ticaret Ltd. Şti. EUDAMED

Active European Union

Ref ARES - BID6004Model ARES - BID6004 - Balloon Inflation Device

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-86989077429740 Basic UDI-DIDate25 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Balloon Inflation Device
Model / Reference
ARES - BID6004 - Balloon Inflation Device, ARES - BID6004
Primary DI / UDI-DI
86989077429740, 86989077474818
Basic UDI-DI
B-86989077429740, B-86989077474818
EMDN Code
C010401020180 Ptca balloon dilatation catheters - accessories
Device Class
Class I
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000029015

Other devices from Ares Medikal Sanayi Ticaret Ltd. Şti.

See all devices from Ares Medikal Sanayi Ticaret Ltd. Şti. →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No