BEUDAMED
    25 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    LOFLO C5 CO2 SENSOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776161958·Stevens Ten Scissors

    ELECSYS DHEA-S

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    PROGES FOLYSIL SILICONE FOLEY CATHETER, STRAIGHT CYLINDRICAL TIP, SILICONE FEMALE FOLEY CATHETER, STRAIGHT CYLINDRICAL,

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

    INSIGNIA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·April 11, 2013

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·April 13, 2011

    ENDEAVOR RX

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·May 28, 2008

    PORTEX® ULTRAPERC® SINGLE DILATOR TUBE

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD; INC.·Product code JOH·October 17, 2019

    ANATOMICAL SHOULDER REVERSE, HUMERAL CUP, 0°, RETRO

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSD·November 21, 2018

    ANATOMICAL SHOULDER REVERSE, SCREW SYSTEM, 4.5-18

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWT·November 21, 2018

    ANATOMICAL SHOULDER REVERSE, HUMERAL INSERT, PE, 36-0

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWS·November 21, 2018

    ANATOMICAL SHOULDER FRACTURE, HUMERAL STEM, 7-130

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWS·November 21, 2018

    PORTEX BLUE LINE ULTRA SUCTIONAID PERCUTANEOUS DILATION TRACHEOSTOMY KIT

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code JOH·October 14, 2019

    BACT/ALERT MP 419744

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC·Product code MDB·December 6, 2019

    BACT/ALERT MP 419744

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC·Product code MDB·December 6, 2019

    BACT/ALERT MP 419744

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC·Product code MDB·December 6, 2019

    BACT/ALERT MP 419744

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC·Product code MDB·December 6, 2019

    BACT/ALERT MP 419744

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC·Product code MDB·December 6, 2019

    BACT/ALERT MP 419744

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC·Product code MDB·December 6, 2019

    BACT/ALERT MP 419744

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC·Product code MDB·December 6, 2019