BEUDAMED
    14 results · 18ms · Sources: EU EUDAMED, US FDA

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    SUPERGLOVES, POWDER FREE NITRILE EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993258·anteriors; shade B3; mould UIM

    ProLift Expandable System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BLOM-SINGER INDWELLING TEP OCCLUDER

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    HARMONY 585 LED

    FDA Adverse Event
    STERIS CORPORATION - MONTGOMERY·Product code FSY·March 7, 2013

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 7, 2011

    DURAL ALPHA INSERT W RIM II/32

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LPH·March 12, 2019

    DURASUL, ALPHA INSERT, HOODED, II/32

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LPH·September 28, 2018

    METASUL, ALPHA INSERT, JJ/28

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·February 4, 2019

    DURASUL, ALPHA INSERT, KK/36

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·March 13, 2018

    COCR HEAD 32/ 0 'M' 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·June 4, 2019

    DURASUL, ALPHA INSERT, LL/36

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·April 29, 2019

    DURASUL, ALPHA INSERT, HOODED, KK/32

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LPH·June 15, 2018