BEUDAMED
    12 results · 29ms · Sources: EU EUDAMED, US FDA

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    ISO-GARD MASK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Gyrus ACMI

    FDA UDI
    Gyrus ACMI, LLC·00821925017092·RICHARDS FLUOROPLASTIC BUCKET HANDLE PROTESIS, ...

    MAXIM VI KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304205529·

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWP·March 31, 2016

    ULTRASONIC TABLETOP DOPPLER; ULTRASONIC TABLETOP DOPPLER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    FULL AUTO WRIST DIGITAL BLOOD PRESSURE MONITOR MODEL# SE-311

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 30, 2015

    COBAS INTEGRA 400 PLUS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JGS·April 27, 2010

    INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 4, 2014

    ALIGN R RETROPUBIC URETHRAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·BARD SHANNON LIMITED·Product code OTN·May 29, 2013

    ARDIS PEEK IMPLANT 10X09X26

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code MAX·May 26, 2011

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 5, 2022