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AQVITOX-D roztok 500 ml, fľaša

by Aqvitox Technology, s.r.o. EUDAMED

Active European Union

Ref 500ml flasa

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8588007405AQVITOXDROZTFW Basic UDI-DIDate29 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2024-MDR/QS-012/A Supplemented

    Quality management system EU MDR

    Notified body
    3EC International a.s. 2265
    Issued
    16 Jul 2025
    Expires
    20 Mar 2029
    Reason
    Other

Specification

EUDAMED

Device Name
Aqvitox - D roztok
Model / Reference
500ml flasa
Primary DI / UDI-DI
08588007405599
Basic UDI-DI
8588007405AQVITOXDROZTFW
Direct Marketing DI
08588007405599
EMDN Code
M04041503 Dressings in solutions, emulsions, gels, powders with synthetic components
Device Class
Class IIb
Market of Registration
Slovakia

Manufacturer details

EUDAMED SRN
SK-MF-000026312

Other devices from Aqvitox Technology, s.r.o.

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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