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Ewing Malonate Broth Modified

by BioMaxima Spółka Akcyjna

Ref PW 3020, BT 5018.05, PW 3167, PS 53- 500, PW 3175

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number59026439ATEMMBRSA Basic UDI-DI Date15 Jul 2025RegisteredStatusActive

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  • Withdrawn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

Trade Name
Ewing Malonate Modified Broth
Device Name
Ewing Malonate Broth Modified
Model / Reference
PW 3020, BT 5018.05, PW 3167, PS 53- 500, PW 3175
Primary DI / UDI-DI
05902643938977, 05902643950139, 05902643940918, 05902643905658, 05902643941601
Basic UDI-DI
59026439ATEMMBRSA, 59026439ABEMMBGH, 59026439ASEMMBNC
EMDN Code
W0104010206, W0104010306, W0104010101
Device Class
Class A
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