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

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    BIOSYS FETAL MONITOR, MODEL IFM-500

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    NANOHYBRID COMPULES 15-.3 Gm (C1)

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77819940081·Nanohybrid Composite contains a new ytterbium f...

    STAGE IV, AIR-FLUIDIZE BED

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PENTAX CYSTOFIBERSCOPE, MODEL FCY-15P

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    GENESIS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 1, 2013

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·February 16, 2011

    PROTECTA XT DR

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code LWS·August 8, 2014