BEUDAMED
    5 results · 55ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    ACCUPROBE GROUP B STREPTOCOCCUS CULTURE ID KIT

    FDA Adverse Event
    Injury ·GEN-PROBE INCORPORATED·Product code MDK·January 26, 2012

    ACCUPROBE GROUP B STREPTOCOCCUS CULTURE ID KIT

    FDA Adverse Event
    Death ·GEN-PROBE INCORPORATED·Product code MDK·April 6, 2010

    APTIMA COMBO 2 ASSAY

    FDA Adverse Event
    Injury ·GEN-PROBE INCORPORATED·Product code LSL·February 24, 2014

    ACCUPROBE GROUP B STREP TEST

    FDA Adverse Event
    GEN-PROBE INCORPORATED·Product code MDK·March 14, 2014

    Accuprobe Group B Streptococcus Culture Identification Test, Catalog Number 2820B, Batch Number 531379, Gen-Probe, Incorporated, San Diego, CA. 92121

    FDA Recall
    Terminated ·Gen-Probe Inc·Product code MDK·May 2, 2007