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Aztreonam 30 (B) E110146

by BioMaxima Spółka Akcyjna

Ref E110146 (W), E110146 (K), E110146 (B), 0009B10, 0009B30, 0009B05

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number59026439BASTATMQX Basic UDI-DI Date7 Jul 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Trade Name
Aztreonam
Device Name
Aztreonam 30 (B) E110146
MIC test AZTREONAM
Model / Reference
E110146 (W), E110146 (K), E110146 (B), 0009B10, 0009B30, 0009B05
Primary DI / UDI-DI
05902643981133, 05902643978133, 05902643900134, 05902643972599, 05902643975095, 05902643970090
Basic UDI-DI
59026439BASTATMQX, 59026439BBMATMJ5
EMDN Code
W0104080502, W0104080501
Device Class
Class B
EU 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