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Orbis Hypodest 3 %, Sodium hypochlorite 3 %, 500 ml

by DNTL Nordic ApS Denmark EUDAMED

Ref R306915 EMDN Q010199

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number571473412042BC Basic UDI-DIDate12 Jan 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Orbis Hypodest 3 %, Sodium hypochlorite 3%, 500 ml
Model / Reference
R306915
Primary DI / UDI-DI
05714734120426
Basic UDI-DI
571473412042BC
EMDN Code
Q010199 Conservative dentistry and endodontics devices - other
Device Class
Class I
Market of Registration
Finland

Manufacturer details

EUDAMED SRN
DK-MF-000013594

Other devices from DNTL Nordic ApS

See all devices from DNTL Nordic ApS →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 50208e55-0652-4d93-a908-bccd3275e7bc 61 fields · synced 22 Oct 2026