BEUDAMED
    13 results · 21ms · 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.
    Filters Regulation: Us FDA ×

    ActiveCare+SFT;ActiveCare+SFT HomeCare, ActiveCare+DTx;ActiveCare+DTx HomeCare

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ProLift Trial

    FDA UDI
    Life Spine, Inc.·00190837087234·

    SMITH & NEWPHEW ULTRABRAID II SUTURE

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

    STERRAD(R) 100NX STERILIZER DUO CYCLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SMARTSET GMV 40G US EO

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code MBB·April 20, 2021

    SMARTSET GMV 40G US EO

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code MBB·April 20, 2021

    SMARTSET GMV 40G US EO

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code MBB·May 11, 2021

    SMARTSET GMV 40G US EO

    FDA Adverse Event
    Injury ·DEPUY CMW - 9610921·Product code MBB·May 11, 2021

    ISOFLEX OPTIM LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC. CRMD·Product code DTB·January 13, 2014

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 30, 2013

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·June 8, 2011

    SMARTSET GMV 40G US EO

    FDA Adverse Event
    Injury ·DEPUY CMW - 9610921·Product code MBB·November 3, 2020

    SMARTSET GMV 40G US EO

    FDA Adverse Event
    Injury ·DEPUY CMW - 9610921·Product code MBB·November 3, 2020