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

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    LUPOTEK KCT

    FDA 510(k)
    FDA Class 2 ·Hematology

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065630·INTRAORAL ELASTICS 2,5 oz 1/8" brown

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481113819·LOCATOR R-Tx Abutment for Regular Internal Conn...

    LOCATOR F-Tx

    FDA UDI
    Zest Anchors, LLC·00840481115349·LOCATOR F-Tx Abutment for Regular Internal Conn...

    RHYTHM OF LIFE, MODEL R0901-05

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (38 CM), MODEL 3555-38; MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (60 CM),

    FDA 510(k)
    FDA Class 2 ·Neurology

    ANESTHESIA MONITOR; BEDSIDE MONITOR, SERIES BSM-5130A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LUX 1440

    FDA Adverse Event
    Malfunction ·PALOMAR MEDICAL TECHNOLOGIES, INC.·Product code GEX·May 5, 2012

    UNKNOWN LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·February 10, 2015

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·December 29, 2015

    LIFESTENT VASCULAR STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code NIP·May 6, 2011

    ATLAS PLUS HF CRT-D

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·May 2, 2013

    PASSPOR V MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·August 18, 2014

    Pronto Series Power Wheelchair, model M50.

    FDA Recall
    Terminated ·Invacare Corporation·Product code ITI·May 2, 2005