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Nutrient S LAB-AGAR™

by BioMaxima Spółka Akcyjna EUDAMED

Active European Union

Ref BT 5116.02, BT 5126.05, BT 5126.01, PP 1503, BT 5126.02

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number59026439ABNUTSMF Basic UDI-DIDate3 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  • Withdrawn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

Trade Name
Nutrient LAB-AGAR™
Device Name
Nutrient S LAB-AGAR™
Model / Reference
BT 5116.02, BT 5126.05, BT 5126.01, PP 1503, BT 5126.02
Primary DI / UDI-DI
05902643947757, 05902643947634, 05902643947610, 05902643930070, 05902643947627
Basic UDI-DI
59026439ABNUTSMF, 59026439ABNUTLY, 59026439APNUTQ2, 59026439ASNUTQP
EMDN Code
W0104010306, W0104010405
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