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Citricadez 20%; Citricadez 50%

by Живас Оод 4 variants

Ref zh042/10/bg/01_50%

Active European Union

CE MDR

Valid until

8 Nov 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier 3EC International a.s.

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/MDR Number38002282404255 Basic UDI-DI 03800228241684UDI-DIDate30 Apr 2025RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2024-MDR/QS-063 Active

    Quality management system EU MDR

    Certifier
    3EC International a.s. 2265
    Issued
    8 Nov 2024
    Expires
    8 Nov 2029

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Citricadez 20%; Citricadez 50%
Model / Reference
zh042/10/bg/01_50%
Primary DI / UDI-DI
03800228241684
Basic UDI-DI
38002282404255
EMDN Code
D99 Disinfectants, antiseptics, sterilising agents and detergents for medical devices - other
Models / Variants
Device Class
Class IIb
EU market of registration
Bulgaria

Manufacturer details

EUDAMED SRN
BG-MF-000019745

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    Class IIb

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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