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IsoDent suojaava suuvesi 250ml

by IsoDent Oy

Ref 6430043960285, 6430043969929

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6430043966430043960285WZ Basic UDI-DI Date25 Oct 2023RegisteredStatusActive

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  • Withdrawn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
IsoDent suojaava suuvesi 250ml
Model / Reference
6430043960285, 6430043969929
Primary DI / UDI-DI
06430043960285, 06430043969929
Basic UDI-DI
6430043966430043960285WZ
Direct Marketing DI
06430043960285
06430043969929
EMDN Code
Q01010403 Dental abrasive and polishing materials
Device Class
Class I
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000023346

Other devices from IsoDent Oy

See all devices from IsoDent Oy →

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