BEUDAMED
    30 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    IBS-B MIS Beveled Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UCP PREGNANCY CASSETTE TEST, DIP/CARD STRIP, HOME PREGNANCY CASSETTE TEST, MIDSTREAM TEST AND DIP/CARD STRIP

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    AUTO-BAND LIGATOR

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

    T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OZO·October 19, 2022

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·December 21, 2015

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·December 21, 2015

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·December 21, 2015

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·December 21, 2015

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·December 21, 2015

    ENTERRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LNQ·November 13, 2008

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·July 22, 2011

    VA LOCKSCR Ø2.4 SELF-TAP L22 TAN

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·July 17, 2013

    MEDTRONIC LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·June 9, 2014

    BONE PLATE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·April 4, 2016

    BONE PLATE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·April 4, 2016

    BONE PLATE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·April 4, 2016

    UNSPECIFIED BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·October 15, 2025

    BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE 5MG/4MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·May 23, 2024

    BONE PLATE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·April 4, 2016

    BONE PLATE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·April 4, 2016