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

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    Mould Applicator Set

    FDA 510(k)
    FDA Class 2 ·Radiology

    INTEGRAL CENTRALIZER HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304223332·

    INTEGRAL HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304208568·

    WIRELESS DR IMAGING OPTION-WDR1

    FDA 510(k)
    FDA Class 2 ·Radiology

    VISION BIOSYSTEMS PROGESTERONE RECEPTOR PGR CLONE 16

    FDA 510(k)
    FDA Class 2 ·Hematology

    ENDO II TAPER INSERT +3MM T1

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 13, 2018

    E-POLY 44MM +3 MROM LNR SZ25

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·March 13, 2018

    ENDO II MOD ENDO HEAD SZ 44

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWL·March 13, 2018

    FRESENIUS 2008K

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·October 7, 2014

    GYNECARE PROLIFT TOTAL PELVIC FLOOR REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·June 11, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 14, 2011