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Orotol ultra

by orochemie GmbH + Co. KG EUDAMED

Active European Union

Ref CDS120A6750

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++EORO0002ADPMR Basic UDI-DIDate2 Dec 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  • Withdrawn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

Device Name
Disinfectants for non-invasive medical devices - Suction System Dis-infection, Powder
Model / Reference
CDS120A6750
Primary DI / UDI-DI
+EOROCDS120A6750
Basic UDI-DI
++EORO0002ADPMR
Direct Marketing DI
+EOROCDS120A6750
EMDN Code
D050101 Peracetic and acetic acid with hydrogen peroxide for the disinfection of medical devices
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006461

Other devices from orochemie GmbH + Co. KG

See all devices from orochemie GmbH + Co. KG →

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