BEUDAMED
    155 results · 25ms · Sources: EU EUDAMED, US FDA

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    Humeris Shoulder

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOMET HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·05019279400799·

    Biomet® Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868308338·

    MEDINAUT KYPHOPLASTY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRANSTEK WRIST BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ZILVER 518 BILIARY SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 21, 2017

    ASR ACETABULAR CUPS 50

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·June 11, 2013

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·June 10, 2011

    ASCENSIA BREEZE (US)

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·September 9, 2008

    ZILVER 635 BILIARY SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 20, 2017

    ZILVER 635 SELF-EXPANDING BILIARY STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 7, 2017

    ZILVER 635 SELF-EXPANDING BILIARY STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FGE·February 28, 2018

    ZILVER 635 BILIARY SELF-EXPANDING STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FGE·February 12, 2018

    ARCOM 32MM RNGLOC LNR HWALL 23

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 9, 2026

    E1 RINGLOC ACETABULAR LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·June 20, 2017

    EXCEED ABT E1 FLNG CUP 32X50MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·March 15, 2019

    ARCOS CON SZ A STD 60MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 28, 2026

    ARCOS STS DIST STEM 13X250MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 28, 2026

    M2A MODULAR HEAD COMPONENT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 30, 2017

    TPRLC 133 FP TYPE1 BM HO 10.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2019