Skip to content

Olympus EndoDis Pro

by Ecolab Deutschland GmbH

Ref 3099120, 3002890, 3100780

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD NumberB-04028163099132 Basic UDI-DI Date17 Mar 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Trade Name
Olympus EndoDis Pro
Olympus Endodis
Device Name
Olympus Endodis -3x2.8l
Model / Reference
3099120, 3002890, 3100780
Primary DI / UDI-DI
04028163099132, 04028163035000, 04028163100791
Basic UDI-DI
B-04028163099132, B-04028163035000, B-04028163100791
EMDN Code
D050101 Peracetic and acetic acid with hydrogen peroxide for the disinfection of medical devices
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000004932

Other devices from Ecolab Deutschland GmbH

See all devices from Ecolab Deutschland GmbH →

Properties

  • Administering Medicine YesEUDAMEDNoEUDAMED

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No