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

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    BICORE SMARTVALVE OCCLUSION VALVE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Disposable Surgical Gown UM-148

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

    ENDOSCOPIC LIGHT SOURCE, MODEL XL300/L5

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

    BASIS¿ SPINAL SYSTEM

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

    PROCISE EZ VIEW

    FDA Adverse Event
    Injury ·ARTHROCARE CORPORATION·Product code KOG·January 15, 2013

    ATTAIN OTW

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code DTB·July 9, 2014

    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

    DYNESIS HA PEDICLE+SET SCR 6.0X40

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code NQP·March 16, 2019

    PENTAX

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

    PENTAX

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