BEUDAMED
    8 results · 34ms · Sources: EU EUDAMED, US FDA

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    FLEX-TECH BALLOON DILATOR

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

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867138414·VOLKMANN BONE HK,9" LNGX 20MM DEEP,SHARP

    VOLKMANN BONE HK,9" LNGX 20MM DEEP,SHARP

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·July 25, 2022

    BIO-MATE PIC CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NEUROSEARCH-4

    FDA 510(k)
    FDA Class 2 ·Neurology

    INTERSTIM

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·November 10, 2010

    LOCKING CAP

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWC·January 23, 2013

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 10, 2014