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Sodium Selenite Broth

by BioMaxima Spółka Akcyjna EUDAMED

Active European Union

Ref PW 4209, PW 4209S, BT 5057.01, PW 3008, PW 3095, PW 3030, BT 5057.02, PS 68- 250, PS 68- 100, PW 3030S, PS 68- 5KG

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number59026439ATSSBRSN Basic UDI-DIDate15 Jul 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • 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

Model / Reference
PW 4209, PW 4209S, BT 5057.01, PW 3008, PW 3095, PW 3030, BT 5057.02, PS 68- 250, PS 68- 100, PW 3030S, PS 68- 5KG
Primary DI / UDI-DI
05902643939707, 05902643939714, 05902643949119, 05902643940055, 05902643940062, 05902643940741, 05902643950207, 05902643989672, 05902643919174, 05902643941472, 05902643924710
Basic UDI-DI
59026439ATSSBRSN, 59026439ABSSBRLG, 59026439ASSSBRSB
EMDN Code
W0104010206, W0104010306, W0104010101
Device Class
Class A
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000039473

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Properties

  • Professional Testing

Other properties (10)

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