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Bacillol 30 Sensitive Foam

by BODE Chemie GmbH EUDAMED

Active European Union

Ref 981699, 981844, 981861, 981839Model 3833

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40316783833LZ Basic UDI-DIDate12 Oct 2022RegisteredStatusActive

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  • Withdrawn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
Bacillol 30 Sensitive
Model / Reference
3833, 981699, 981844, 981861, 981839
Primary DI / UDI-DI
04031678080328, 04031678079803, 04031678079711, 04031678079728
Basic UDI-DI
40316783833LZ
Unit of Use DI
04031678080311, 04031678079797
EMDN Code
D0701 Ethanol for the disinfection of medical devices
Device Class
Class IIa
Market of Registration
Portugal
Hungary
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005851

Other devices from BODE Chemie GmbH

See all devices from BODE Chemie GmbH →

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