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Ares

by Ares Medikal Sanayi Ticaret Ltd. Şti. Türkiye EUDAMED

Ref ARES - HCT10038 Model ARES - HCT10038

EMDN F900201

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-86989077479240 Basic UDI-DIDate15 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 24 Oct 2026

Device Name
Hemodialysis catheter kit
Model / Reference
ARES - HCT10038
Primary DI / UDI-DI
86989077479240
Basic UDI-DI
B-86989077479240
EMDN Code
F900201 Temporary hemodialysis catheters and kits
Device Class
Class IIa
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 7f3a73df-ddd7-4d0a-9369-44696a61e2d7 61 fields · synced 24 Oct 2026