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Kompres 10 cm x 20 cm

by A.C.S. Tibbi̇ Teksti̇l Ürünleri̇ San.ve Ti̇c. Ltd.şti̇

Ref ACS-00-278, A-141

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number869891806K-ACS02TJ Basic UDI-DI Date19 Apr 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Trade Name
Kompres 10 cm x 20 cm
Kompres 10 cm x 20 cm Radyopak Şeritli
Device Name
Kompres
Model / Reference
ACS-00-278, A-141
Primary DI / UDI-DI
08698918063303, 08698918060876
Basic UDI-DI
869891806K-ACS02TJ, 869891806S-ACS-R4
EMDN Code
M0201020102, M0201030202
Device Class
Class I
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000034362

Other devices from A.C.S. Tibbi̇ Teksti̇l Ürünleri̇ San.ve Ti̇c. Ltd.şti̇

See all devices from A.C.S. Tibbi̇ Teksti̇l Ürünleri̇ San.ve 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