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Komprese od gaze nesterilne, 100 kom

by Project Pharmacy Doo 60 variants

Ref 13KN7.5X7.5/16

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 Number860601005-COMPRESS-NS-PQ Basic UDI-DI 08606010058486UDI-DIDate14 Oct 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  • Withdrawn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
Komprese od gaze nesterilne, 100 kom
Model / Reference
13KN7.5X7.5/16
Primary DI / UDI-DI
08606010058486
Basic UDI-DI
860601005-COMPRESS-NS-PQ
EMDN Code
M0201050102 Cotton gauze pads, without x-ray detectable thread, non-sterile
Device Class
Class I
EU market of registration
Croatia

Manufacturer details

EUDAMED SRN
RS-MF-000030122
Authorised representative
Salus Cons Kft. HU-AR-000006177

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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