BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    R AND D BATTERY REPLACEMENT

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Freespira Breathing System

    FDA 510(k)
    FDA Class 2 ·Neurology

    ULTRAPRO MESH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON SARL·Product code OTN·September 27, 2016

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·January 29, 2013

    TRANSPORT SERIES

    FDA Adverse Event
    Malfunction ·STRYKER CORP, MEDICAL DIVISION·Product code FPO·December 14, 2010

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 14, 2014

    S-ROM M HEAD 36MM +6

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·May 29, 2012

    PINNACLE MTL INS NEUT36IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·May 29, 2012

    PINNACLE SECTOR II CUP 58MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·May 29, 2012

    S-ROM*SLEEVE PRX ZTT, 18D-LRG

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·May 29, 2012

    VERSYS FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code LPH·February 25, 2016