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

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    DIGITIZER DIRECTOR (HSC025-01)

    FDA 510(k)
    FDA Class 1 ·Radiology

    artegral

    FDA UDI
    Merz Dental GmbH·D7091972191·posteriors; shade BL4; size XL; lower jaw

    STERIZONE VP4 Sterilizer

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CLEARVISION NUCLEAR MEDICINE IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    IBP ELBOW INTERLOK FINISH ULNAR COMPONENT STANDARD LEFT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·June 14, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·February 9, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·March 2, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·February 9, 2017

    FLOGARD

    FDA Adverse Event
    Malfunction ·SHARP CORPORATION OSAKA JAPAN·Product code FRN·February 21, 2013

    BIOLOX CERAMIC HEAD 36MM + 0

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·January 7, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    MEDTRONIC MINIMED·Product code OYC·July 31, 2014