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Sabouraud Dextrose with Chloramphenicol LAB-AGAR™

by BioMaxima Spółka Akcyjna EUDAMED 7 variants

Active European Union

Ref PP 1231, BT 5108.05, PP 1230, BT 5108.02, PS 32- 500, PS 32- 25KG

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number59026439APSDCCN4 Basic UDI-DIDate14 Jul 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Trade Name
Sabouraud Dextrose LAB-AGAR™ with Chloramphenicol
Sabouraud Dextrose LAB-AGAR™
Sabouraud Dextrose with Chloramphenicol LAB-AGAR™
Model / Reference
PP 1231, BT 5108.05, PP 1230, BT 5108.02, PS 32- 500, PS 32- 25KG
Primary DI / UDI-DI
05902643930315, 05902643948624, 05902643930261, 05902643948617, 05902643908826, 05902643924949
Basic UDI-DI
59026439APSDCCN4, 59026439ABSDCLHU, 59026439APSADEMU, 59026439ASSDCCP5, 59026439ASSADENV
EMDN Code
W0104010405, W0104010306, W0104010101
Device Class
Class A
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000039473

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Properties

  • Animal Tissues NoEUDAMEDYesEUDAMED
  • Microbial Substances NoEUDAMEDYesEUDAMED
  • Professional Testing

Other properties (8)

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