BEUDAMED
    11 results · 24ms · Sources: EU EUDAMED, US FDA

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    OLYMPUS ULTRASONIC PROBES

    FDA 510(k)
    FDA Class 2 ·Radiology

    PERRY SUTURING SET W/ANESTHETIC

    FDA 510(k)

    HERCULES MODEL 5000 AND 5040 ND:YAG LASER SYSTEMS

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

    BIO PLUG BONE CEMENT RESTRICTOR

    FDA Adverse Event
    Death ·BIOMET ORTHOPEDICS·Product code JDS·October 17, 2017

    UNKNOWN ACETABULAR SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 2, 2019

    LARGE NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·February 5, 2013

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 3, 2011

    ENSEAL G2 CURVED JAW

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·July 18, 2014

    FEMORAL STEM CMK OC MODULAR CEMENTED

    FDA Adverse Event
    Death ·BIOMET FRANCE S.A.R.L.·Product code JDI·October 30, 2017

    STAINLESS STEEL MODULAR HEAD

    FDA Adverse Event
    Death ·BIOMET FRANCE S.A.R.L.·Product code JDI·October 30, 2017

    RINGLOC HIP SYSTEM ACETABULAR BI-POLAR CUP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·October 17, 2017