BEUDAMED
    6 results · 26ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    MONO 2 OXYGEN MONITOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RF GENERATORS, DISPOSABLE CARTRIDGE KIT, DISPOSABLE CARTRIDGE, REUSABLE HANDLE, DISOISABLE HANDPIECE REUSABLE TELESCOPE

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

    ADVANCED PERFUSION SYSTEM 1 (APS1) TUBE CLAMP ASSEMBLY, ROLLER PUMP 6 INCH CLASSIC COLOR,

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 17, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Injury ·MEDTRONIC MILACA INC.·Product code DTE·October 31, 2012

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·August 17, 2010