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Zilvernitraatstift 95% in blauw plastic huls

by Mainit-BV EUDAMED

Active European Union

Ref 226511

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number87202994228ZVNTMAINITPNGY Basic UDI-DIDate12 Nov 2025RegisteredStatusActive

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  • Withdrawn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)
  • BE25/00000286 Issued

    Quality management system EU MDR

    Notified body
    Notified body 1639
    Issued
    4 Nov 2025
    Expires
    4 Nov 2030

Specification

EUDAMED

Device Name
Mainit Zilvernitraat
Model / Reference
226511
Primary DI / UDI-DI
08720299422834
Basic UDI-DI
87202994228ZVNTMAINITPNGY
Direct Marketing DI
08720299422834
EMDN Code
M0412 Dressings for the treatment of warts, corns and calluses
Device Class
Class IIa
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000012155

Other devices from Mainit-BV

Properties

Show 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