BEUDAMED
    14 results · 32ms · Sources: EU EUDAMED, US FDA

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    IQ NASAL MASK, MODEL P/N 50160

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993269·anteriors; shade B4; mould BM

    UroLift System (UL400)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PROCEDURE REHEARSAL STUDIO

    FDA 510(k)
    FDA Class 2 ·Radiology

    UNKNOWN DEPUY BONE CEMENT

    FDA Adverse Event
    Injury ·DEPUY CMW 9610921·Product code LOD·March 7, 2013

    9900

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

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 8, 2014

    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