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REYA Reya Trombektomi Sistem VI

by Fg Grup Sağlik İnşaat Hari̇ta Mi̇marlik Mühendi̇sli̇k Elektroni̇k Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ EUDAMED

Active European Union

Ref ATA0012

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08680400433572 Basic UDI-DIDate21 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Reya Trombektomi Sistem VI
Model / Reference
ATA0012
Primary DI / UDI-DI
08680400433572
Basic UDI-DI
B-08680400433572
EMDN Code
C01050299 Intravascular embolic protection catheters and systems - other
Device Class
Class III
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000027182

Other devices from Fg Grup Sağlik İnşaat Hari̇ta Mi̇marlik Mühendi̇sli̇k Elektroni̇k Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

See all devices from Fg Grup Sağlik İnşaat Hari̇ta Mi̇marlik Mühendi̇sli̇k Elektroni̇k Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ →

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