BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    VERTICAL LIFT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    K083526

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·May 7, 2018

    PROXIMATE ILS CIRCULAR STAPLES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.·Product code GAG·June 7, 2006

    TIBIAL NAIL, STANDARD 10X390 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·March 17, 2010

    TRILOGY 100 VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Codman Electrosurgical Generator, Foot Pedal

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

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 20, 2021

    PROXIMATE ILS CIRCULAR STAPLERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.·Product code GAG·June 7, 2006

    LIGASURE BLUNT TIP LAP SEALER/DIVIDER

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code GEI·June 26, 2014

    CANCELLOUS BONE SCREW 6.5X35MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HRS·February 28, 2013

    ASR ACETABULAR CUPS 52

    FDA Adverse Event
    Injury ·DEPUY INT'L LTD·Product code KWA·January 31, 2011