BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    ENDOPATH DISPOSABLE PNEUMOPERITONEUM NEEDLE

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

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909108752·REVELATION DIAMOND 863-014C - 5 PACK

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756379595·ENT MAJOR PACK

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450230794·

    HYCARE LATEX EXAMINATION GLOVE, POWDERED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CENTRICITY PACS

    FDA 510(k)
    FDA Class 2 ·Radiology

    REVERSE SHOULDER SYSTEM LAT. GLENOSPHERE 39X27

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSD·March 17, 2021

    REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER 39/+0MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·June 16, 2020

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·November 23, 2010

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·January 11, 2013

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·July 2, 2014

    PORTEX BLUE LINE ULTRA SUCTIONAID

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code JOH·August 8, 2019