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Medione

by Avrasyamed Medi̇kal Tibbi̇ Ci̇h. Ve Ür. Paz. San. Ve Diş Ti̇c. Ltd. Şti̇. 3 variants

Ref TRQ-2022

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08682754922238 Basic UDI-DI 08682754922238UDI-DIDate14 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Automatic Tourniquet Device
Model / Reference
TRQ-2022
Primary DI / UDI-DI
08682754922238
Basic UDI-DI
B-08682754922238
EMDN Code
Z12139006 Pneumatic tourniquets
Device Class
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000040217

Other devices from Avrasyamed Medi̇kal Tibbi̇ Ci̇h. Ve Ür. Paz. San. Ve Diş Ti̇c. Ltd. Şti̇.

See all devices from Avrasyamed Medi̇kal Tibbi̇ Ci̇h. Ve Ür. Paz. San. Ve Diş Ti̇c. Ltd. Şti̇. →

Properties

  • Measuring Function

Other properties (10)

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