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Mainit Zilvernitraat 75% w/w Caustic Applicator 15cm disp. Koker

by Mainit-BV

Ref 226505

Active European Union

CE MDR

Valid until

4 Nov 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS Belgium NV

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/MDR Number87202994228ZVNTMAINITX5 Basic UDI-DI 08720299422810UDI-DIDate13 Nov 2025RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • BE25/00000286 Active

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    4 Nov 2025
    Expires
    4 Nov 2030

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Mainit Zilvernitraat
Model / Reference
226505
Primary DI / UDI-DI
08720299422810
Basic UDI-DI
87202994228ZVNTMAINITX5
Direct Marketing DI
08720299422810
EMDN Code
M0412 Dressings for the treatment of warts, corns and calluses
Device Class
Class IIa
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000012155

Other devices from Mainit-BV

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