BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    PENTAX NASO-PHARYNGO-LARYNGOSCOPE FNL-15P2/15RP2

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    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

    SINGLE STEP BIOPSY DEVICE, SINGLE STEP SURGICAL HANDLE, SINGLE STEP DRIVER, SINGLE STEP HOLDERS

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

    LEW MDI O-BALL COLLARED IMPLANT,

    FDA 510(k)
    FDA Class 2 ·Dental

    BASIS¿ SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC·Product code KWP·July 19, 2012

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 29, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010

    2.7MM/3.5MM LCP LATERAL DISTALFIBULA PLATE 5H/LEFT/99MM

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code HRS·January 18, 2013