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

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    Filters Regulation: Us FDA ×

    Orapeutic

    FDA 510(k)
    FDA Unclassified ·Unknown

    Bernafon

    FDA UDI
    Bernafon AG·05711584087077·ZR3, KIT IIC 10 75 BL ZERENA 3

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111442285·STILLE-BARRAYA FORCEPS 3X4 7 INCHES

    ANASTOCLIP MODELS 4001-01, 4000-02, 4000-03, 4000-04, 4004-01, 4004-02, ANASTOCLIP

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

    COOL LINE CATHETER, MODEL CL-2295A, ICY CATHETER, MODEL IC-3893A AND QUATTRO CATHETER, MODEL IC-4593

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SIMPLE PREP CARBIDE

    FDA Adverse Event
    Injury ·COLTENE WHALEDENT INC.·Product code EJL·February 3, 2022

    SMARTSET GMV 40G US EO

    FDA Adverse Event
    Injury ·9610921 DEPUY CMW·Product code MBB·October 22, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 27, 2013

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·July 22, 2011

    DAVINCI X

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 17, 2026