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Ares

by Ares Medikal Sanayi Ticaret Ltd. Şti. Türkiye EUDAMED

Ref BID3525KPPT Model BID6001

EMDN C010402020101

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-86989077507400 Basic UDI-DIDate11 Jun 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 24 Oct 2026

Device Name
Balloon Inflation Device
Model / Reference
BID6001, BID3525KPPT
Primary DI / UDI-DI
86989077507400
Basic UDI-DI
B-86989077507400
EMDN Code
C010402020101 PTA balloon dilatation catheters
Device Class
Class I
Market of Registration
Italy

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 86989077507400|B-86989077507400 61 fields · synced 24 Oct 2026