BEUDAMED
    35 results · 36ms · Sources: EU EUDAMED, US FDA

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    RANDOX FERRITIN

    FDA 510(k)
    FDA Class 2 ·Immunology

    Preat

    FDA UDI
    Preat Corporation·00842092169599·NobelBiocare™ Tri-Lobe-compatible WP X 6.0mm En...

    PowerPICC SOLO

    FDA UDI
    Bard Access Systems, Inc.·00801741129674·Catheter Placement Kit

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092117521·NobelBiocare™ Tri-Lobe-compatible WP X 6mm Tita...

    APPLIANCE, FIXATION, NAIL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KTT·August 18, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·January 5, 2016

    CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    METRISCAN BONE DENSITY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES BETTLACH·Product code HWC·September 23, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES MEZZOVICO·Product code HWC·September 1, 2015

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·January 26, 2018

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·January 25, 2018

    NOVA MAX PLUS BLOOD GLUCOSE METER

    FDA Adverse Event
    Malfunction ·NOVA BIOMEDICAL CORP.,·Product code NBW·December 7, 2016

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·July 10, 2024

    LCP 4.5/5 BROAD 18HO L332 TI

    FDA Adverse Event
    Injury ·SYNTHES·Product code KTT·December 12, 2012

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·March 12, 2013

    EXCLAIM 8 SURGICAL LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 16, 2011

    GE STENOSCOPE

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·February 21, 2008

    LOCKSCR Ø5 SELF-TAP L55 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code KTT·April 11, 2013

    NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662

    FDA Recall
    Open, Classified ·Preat Corp·Product code NHA·June 25, 2025