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

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    GUIDE-TECH ENCAPSULATED GUIDEWIRE

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

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867138421·VOLKMANN RETRTR,8.5"LG 4 PRONG SEMI SHRP

    MEDIJECT DISPOSABLE SYRINGES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RX 90 ACETABULAR COMPONENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACTIVA PC

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

    MATNEU SCR Ø1.5 SELF-DRILL L4 TAN 4U I/C

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JEY·January 23, 2013

    12FR CORFLO ULTRA NASOGASTRIC TUBE

    FDA Adverse Event
    Injury ·CORPAK MEDSYSTEMS·Product code KNT·July 1, 2014