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Medione

by Avrasyamed Medi̇kal Tibbi̇ Ci̇h. Ve Ür. Paz. San. Ve Diş Ti̇c. Ltd. Şti̇. 13 variants

Ref AVR-CUFF S044Model AVR-CUFF S008

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8682754922010256 Basic UDI-DI 08682754922382UDI-DIDate13 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
8'' Reusable Single Cuff 8”L x 2”W One Chamber
Model / Reference
AVR-CUFF S008, AVR-CUFF S044
Primary DI / UDI-DI
08682754922382
Basic UDI-DI
8682754922010256
EMDN Code
Z12139006 Pneumatic tourniquets
Device Class
Class I
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

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No