Skip to content

Mueller Hinton Broth

by G. PAPANIKOLAOU & CO. LP - Bioprepare 2 variants

Ref 080079Model MUELLER HINTON BROTH 080079

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number52120377080079EX Basic UDI-DI 05212037700531UDI-DIDate1 Sep 2026RegisteredStatusActive

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  • Withdrawn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

Model / Reference
MUELLER HINTON BROTH 080079, 080079
Primary DI / UDI-DI
05212037700531
Basic UDI-DI
52120377080079EX
EMDN Code
W0104010206 Media in tubes (solid & liquid)
Device Class
Class A
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
EL-MF-000055282

Other devices from G. PAPANIKOLAOU & CO. LP - Bioprepare

See all devices from G. PAPANIKOLAOU & CO. LP - Bioprepare →

Properties

  • Sterile
  • Reagent
  • Professional Testing

Other properties (8)

  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No