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Ares

by Ares Medikal Sanayi Ticaret Ltd. Şti. Türkiye EUDAMED

Ref ARES - BID6002Model ARES - BID6002 - İndeflatör

EMDN C010401020180

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-86989077437806 Basic UDI-DIDate14 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Balloon inflation device
Model / Reference
ARES - BID6002 - İndeflatör, ARES - BID6002
Primary DI / UDI-DI
86989077437806
Basic UDI-DI
B-86989077437806
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 & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 9dcce2ae-ddcd-4978-8b09-37b9aabdbf27 61 fields · synced 22 Oct 2026