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Agar Sange Brucella Cu Hemina Si Vitamina K1

by Deltarom SRL

Ref 341251, 3412525, 341255

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

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/IVDR Number594054038AGARSANGEBRU01U9 Basic UDI-DI Date16 Jul 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Model / Reference
341251, 3412525, 341255
Primary DI / UDI-DI
05940540383186, 05940540383179, 05940540383162
Basic UDI-DI
594054038AGARSANGEBRU01U9, 594054038AGARSANGEBRU12UE, 594054038AGARSANGEBRUELXR
EMDN Code
W0104010405, W0104010306, W0104010101
Device Class
Class A
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
RO-MF-000035924

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Properties

  • Animal Tissues NoEUDAMEDYesEUDAMED
  • Reagent
  • Professional Testing

Other properties (8)

  • Sterile: No
  • Human Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No