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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    MEC INTRAMEDULLARY ROD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELASTICS

    FDA UDI
    Gc Orthodontics America Inc.·E53585044111111·ELASTICS HV 4MM 6 OZ Trumpet 3/16 (NEON)

    TAPER 2 POROUS FEMORAL STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Volcano iFR Modality, iFR Scout feature

    FDA 510(k)
    FDA Class 2 ·Radiology

    PRIMORIS HIP STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 5, 2016

    PRIMORIS FEMORAL STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·October 3, 2017

    PRIMORIS NECK PROSTH BM SZ 26

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 4, 2016

    PRIMORIS HIP STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 5, 2016

    PRMRS NCK STEM TI BM SZ 24 RSA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·June 23, 2016

    TAPERLOC LAT COCR 10MM T1

    FDA Adverse Event
    Death ·BIOMET UK LTD.·Product code JDI·March 20, 2026

    TPRLOC COCR CMTD STEM T1 7.5MM

    FDA Adverse Event
    Death ·BIOMET UK LTD.·Product code JDI·March 20, 2026

    UNKNOWN PRIMORIS HIP

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 4, 2016

    PRMRS NCK STEM TI BM SZ 24 RSA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWY·April 13, 2018

    HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·May 15, 2014

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code MMI·October 1, 2010

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·November 26, 2012

    PRIMORIS NECK PROSTHESIS TI BM SIZE 26

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·November 9, 2017

    UNKNOWN PRIMORIS HIP

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 4, 2016

    UNKNOWN PRIMORIS HIP

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 5, 2016

    PRMRS NCK STEM TI BM SZ 24 RSA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·April 13, 2018