BEUDAMED
    207 results · 130ms · Sources: EU EUDAMED, US FDA

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    ENDO CLIP 5MM CLIP APPLIER

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code FZP·April 10, 2014

    DST SERIES* EEA* ORVIL* 25 MM DEVICE

    FDA Adverse Event
    Injury ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDW·June 4, 2014

    IDRIVE ULTRA POWERED HANDLE 1

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDW·May 12, 2014

    ENDO GIA ADAPTER STANDARD

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDW·May 2, 2014

    ENDOSTITCH 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code KOG·June 27, 2014

    IDRIVE ULTRA POWERED HANDLE 1

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDW·June 2, 2014

    ENDO GIA ROTICULATOR 60-3/5 SULU

    FDA Adverse Event
    Injury ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDW·May 12, 2014

    EGIA ULTRA UNIVERSAL STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDW·May 12, 2014

    VLOC 180 ESTITCH ABS 0 8 LOOP

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code KOG·May 29, 2014

    ENDO CLIP II MED/LRG 10MM PISTOL GRIP

    FDA Adverse Event
    Injury ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code FZP·April 4, 2014

    EGIA 45 ARTICULATING VAS/MED SULU

    FDA Adverse Event
    Injury ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDW·June 25, 2014

    EGIA ULTRA UNIVERSAL STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GAG·June 25, 2014

    DST SERIES EEA ORVIL 25MM DEVICE

    FDA Adverse Event
    Injury ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GAG·April 25, 2014

    IDRIVE ULTRA POWERED HANDLE 1

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDW·June 12, 2014

    ENDOCLIP III 5MM APPLIER W/ HEMOSTAY CLIP

    FDA Adverse Event
    Injury ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDO·April 25, 2014

    33 HEMORRHOID STAPLER 3.5MM STAPLES

    FDA Adverse Event
    Injury ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GAG·May 9, 2014

    ENDO GIA MEDIUM/THICK RADIAL RELOAD

    FDA Adverse Event
    Injury ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDW·April 30, 2014

    SIZE 0 8 PBT RELOAD WITH LOOP

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code KOG·June 27, 2014

    AUTOSONIX ULTRA SHEARS LONG

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code LFL·May 2, 2014

    IDRIVE ULTRA POWERED HANDLE 1

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDW·June 12, 2014