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BIOSYNEX AMPLIQUICK Fecal Bacteriology

by Biosynex 3 variants

Ref 3150046_BLK96Model BIOSYNEX AMPLIQUICK Fecal Bacteriology

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 Number353267F00188P98 Basic UDI-DI 03532678607863UDI-DIDate5 Mar 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  • Withdrawn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
BIOSYNEX AMPLIQUICK Fecal Bacteriology, 3150046_BLK96
Primary DI / UDI-DI
03532678607863
Basic UDI-DI
353267F00188P98
EMDN Code
W0105070504 Gastrointestinal infections - multiplex na reagents
Device Class
Class C
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000014073

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See all devices from Biosynex →

Properties

  • Animal Tissues
  • Microbial Substances
  • Reagent
  • Professional Testing

Other properties (7)

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