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Ss Lab-Agar™

by BioMaxima Spółka Akcyjna 2 variants

Ref PP 1250, PS 17- 500, BT 5120.05, BT 5120.02, BT 5120.01, PS 17- 5KG

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 Number59026439APSASHPF Basic UDI-DI Date14 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  • Withdrawn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
Salmonella Shigella LAB-AGAR™
Device Name
Ss Lab-Agar™
Model / Reference
PP 1250, PS 17- 500, BT 5120.05, BT 5120.02, BT 5120.01, PS 17- 5KG
Primary DI / UDI-DI
05902643930322, 05902643908949, 05902643948808, 05902643948792, 05902643948785, 05902643924628
Basic UDI-DI
59026439APSASHPF, 59026439ASSASHQG, 59026439ABSASHJM
EMDN Code
W0104010405, W0104010101, W0104010306
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