BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    ACID HEMOGLOBIN KIT

    FDA 510(k)
    FDA Class 2 ·Hematology

    UNIFOCAL 2-UNIPOLAR & BIPOLAR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    CRC PC Smart Chamber K1

    FDA 510(k)
    FDA Class 2 ·Radiology

    NOTINGHM SHLDR HUM HEAD 48X17 OFFSET

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWS·January 19, 2016

    ASAHI APS DIALYZERS

    FDA Adverse Event
    Injury ·ASAHI KASEI MEDICAL CO., LTD.·Product code KDI·March 1, 2013

    ASKU

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·February 15, 2011

    CAPSURE SENSE

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    GORE® DUALMESH® BIOMATERIAL

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code FTL·November 12, 2020

    GORE® DUALMESH® BIOMATERIAL

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code FTL·November 12, 2020

    COD.712 TOP CIRC.RACC.CARDIO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTN·December 15, 2011