BEUDAMED
    62 results · 26ms · Sources: EU EUDAMED, US FDA

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    GE LOGIQ P6

    FDA 510(k)
    FDA Class 2 ·Radiology

    AIRCAST, MODEL #3011

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MAMMOTOME HAND HELD PROBE, MODEL MHH8

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·November 29, 2019

    WAVEWRITER ALPHA?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 28, 2026

    CAPSTONE VERTEBRAL BODY SPACER

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·July 3, 2017

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code KWP·November 14, 2018

    FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC P

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·January 22, 2020

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·February 22, 2021

    CAPSTONE CAGE

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code MAX·November 19, 2015

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·October 26, 2018

    CAPSTONE VERTEBRAL BODY SPACER

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MAX·July 2, 2009

    CAPSTONE SYSTEM

    FDA Adverse Event
    Malfunction ·SOFAMOR DANEK DEGGENDORF GMBH·Product code MQP·September 3, 2010

    CAPSTONE® SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·April 17, 2014

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·October 18, 2017

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MAX·December 21, 2009

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·April 23, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 1, 2011

    TENDRIL DX

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·July 11, 2008

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MAX·October 10, 2014