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Compress Gel

by Aktaş Sağlik Kozmeti̇k Ve Temi̇zli̇k Ürünleri̇ San. Ti̇c. Ltd. Şti̇. 2 variants

Ref AKT25-09Model 27x35 CM

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number868078904044ATC01104304U Basic UDI-DI 08680789040446UDI-DIDate8 May 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  • Withdrawn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
DERMOKON - 27x35 CM - KOMPRES JEL
Model / Reference
27x35 CM, AKT25-09
Primary DI / UDI-DI
08680789040446
Basic UDI-DI
868078904044ATC01104304U
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000054140

Other devices from Aktaş Sağlik Kozmeti̇k Ve Temi̇zli̇k Ürünleri̇ San. Ti̇c. Ltd. Şti̇.

See all devices from Aktaş Sağlik Kozmeti̇k Ve Temi̇zli̇k Ürünleri̇ San. 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