BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    FLOSENSE, MODEL 29-8010

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CYBER SURGICAL LASER FAMILY INCLUDING: CYBER TM, CYBER GREEN, CYBER GREEN TM

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

    Bella-mu

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEO·June 19, 2006

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·March 6, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·August 8, 2014