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Sorelex 10 x 10 cm, 10 pcs

by Contipro a.s.

Model Sorelex 10x10 (10pcs)

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-SorelexJY Basic UDI-DI D-SorelexJYUDI-DIDate25 Mar 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  • Withdrawn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
Wound-nonadherent dressing, permeable, antimicrobial
Model / Reference
Sorelex 10x10 (10pcs)
Primary DI / UDI-DI
D-SorelexJY
Basic UDI-DI
B-SorelexJY
EMDN Code
M040412 Antiseptics-based dressings
Device Class
Class III
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000014702

Other devices from Contipro a.s.

See all devices from Contipro a.s. →

Properties

  • Sterile
  • Incorporates Medicinal Product

Other properties (9)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No