BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    IMMULITE THEOPHYLLINE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    EMIT(R) II 9 CANNABINOID NEGATIVE CALIBRA/CONTROLS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    HEMOR-ICE

    FDA 510(k)
    FDA Unclassified ·Unknown

    DEXON SUTURE

    FDA Adverse Event
    Injury ·SHERWOOD DAVIS AND GECK·Product code GAO·May 20, 1998

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWP·February 11, 2013

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 24, 2014

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 10, 2011

    BD¿ CHOCOLATE AGAR (GC II AGAR WITH ISOVITALEX¿)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSO·July 15, 2022

    BD¿ CHOCOLATE AGAR (GC II AGAR WITH ISOVITALEX¿), PLATE, 90 MM X 120

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSO·March 29, 2022

    PLATE CHOCO GC AGAR W/ISOVITALEX 90MM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSO·June 1, 2021