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Bacillol Tissues

by BODE Chemie GmbH EUDAMED

Active European Union

Ref 975680, 975683, 982137Model 2658

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40316782658LY Basic UDI-DIDate27 Apr 2023RegisteredStatusActive

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  • Withdrawn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 AF
Model / Reference
2658, 975680, 975683, 982137
Primary DI / UDI-DI
04031678043156, 04031678043187, 04031678091225
Basic UDI-DI
40316782658LY
Unit of Use DI
04031678043149, 04031678043170
EMDN Code
D0799 Alcohols for the disinfection of medical devices - other
Device Class
Class IIa
Market of Registration
Greece
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