Skip to content

Trehalose Broth

by BioMaxima Spółka Akcyjna 3 variants

Ref BT 5092.02, BT 5092.05

Trehalose Broth (BT 5092.02) is a Class A device made by BioMaxima Spółka Akcyjna, registered in EUDAMED on 7 Jul 2025 (Basic UDI-DI 59026439ABTRBRLJ), active as of 25 Oct 2026.

Active European Union

CE IVDR

Valid until

No date given

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

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number59026439ABTRBRLJ Basic UDI-DI Date7 Jul 2025RegisteredStatusActive

Official records

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  • Withdrawn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

Device name
Trehalose Broth
Model / reference
BT 5092.02, BT 5092.05
Primary DI / UDI-DI
05902643949379, 05902643951099
Basic UDI-DI
59026439ABTRBRLJ
EMDN code
W0104010306 Culture media in bottles
Device class
Class A
EU registration type
Standard device
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000039473

Similar devices in this category

Other devices filed under CULTURE MEDIA IN BOTTLES.

Other devices from BioMaxima Spółka Akcyjna

See all devices from BioMaxima Spółka Akcyjna →

Properties

  • Professional testing
Other properties (12, all answered No)