BEUDAMED
    15 results · 23ms · Sources: EU EUDAMED, US FDA

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    ClearPath Aligner

    FDA 510(k)
    FDA Class 2 ·Dental

    INTEGRAL CENTRALIZER HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304223271·

    INTEGRAL HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304208537·

    K162309

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code PGW·November 14, 2019

    MODIFICATION TO ANGIODYNAMICS PROFILER PTA BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KD-5966 SERIES FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDO II HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWL·March 10, 2017

    ENDO II TAPER INSERT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWL·March 10, 2017

    INTEGRAL IMPACT DISTAL CENTRALIZER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWL·March 10, 2017

    ADAPTA SR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·October 10, 2014

    ACCU-CHEK ® PERFORMA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 11, 2013

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 14, 2011

    ALLY WIRE/PIGTAIL 16G COCR

    FDA Adverse Event
    Malfunction ·BIOMET TRAUMA·Product code HRS·January 27, 2017

    UNKNOWN HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 5, 2019

    ALLY WIRE/PIGTAIL 16G COCR

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HRS·January 27, 2017