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Detroprep Wipes 2% Chg 70% Ipa

by Detro Healthcare Ki̇mya Sanayi̇ Anoni̇m Şi̇rketi̇

Ref S-M.DET.2.0130Model Detroprep Wipes 2% CHG, 70% IPA 100 pcs

Active European Union

CE MDR

Valid until

16 Jun 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SZUTEST Konformitätsbewertungsstelle GmbH

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 Number868009710TF05GR Basic UDI-DI 08684539642874UDI-DIDate18 Jun 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2975-MED-2616801 Active

    Quality management system EU MDR

    Certifier
    SZUTEST Konformitätsbewertungsstelle GmbH 2975
    Issued
    17 Jun 2026
    Expires
    16 Jun 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Detroprep Wipes 2% CHG, 70% IPA
Model / Reference
Detroprep Wipes 2% CHG, 70% IPA 100 pcs, S-M.DET.2.0130
Primary DI / UDI-DI
08684539642874
Basic UDI-DI
868009710TF05GR
EMDN Code
D02010199 Chlorhexidine for the disinfection of medical devices - other
Device Class
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000022410

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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