BEUDAMED
    6 results · 27ms · 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.
    Filters Regulation: Us FDA ×

    GONOSPOT* DNA PROBE CULTURE CONFIRMATION TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PRECICE System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PARAGON ELECTROPHORESIS LACTATE REAG.KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·May 23, 2014

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·December 13, 2012

    WOUND VAC

    FDA Adverse Event
    Malfunction ·KCI·Product code OMP·September 27, 2010