BEUDAMED
    7 results · 19ms · 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 ×

    PHOTOTHERAPEUTIX MODEL 800B

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PERIFIX CATHETER CONNECTOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VITEK 2 AST YS FLUCYTOSINE, VITEK 2 AST YEAST FLUCYTOSINE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    VITEK® 2 AST-YS08 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code NGZ·January 11, 2018

    V-60 BIPAP

    FDA Adverse Event
    Malfunction ·RESPIRONICS·Product code MNT·June 30, 2014

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·January 29, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·December 21, 2010