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

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    SELF-CURING HARD DENTURE LINER

    FDA 510(k)
    FDA Class 2 ·Dental

    Deltaven Fast Flash

    FDA UDI
    DELTA MED SPA·08032248382060·Safety IV catheter in PUR with closed system, d...

    PEDICLE SCREW MUST COMBINED SETSCREW H4-T27 - (6X)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·March 13, 2019

    WAVE FORM MANUFACTURING PROLASE GENERAL SHAPED FIBER

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

    DIGITAL AUTOMATIC WRIST BLOOD PRESSURE MONITOR WBPM15 SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PUREPOINT LIO

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQF·April 10, 2014

    HEARTSTART ONSITE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 2, 2012

    IMPLANTIUM

    FDA Adverse Event
    Injury ·DENTIUM USA·Product code DZE·August 26, 2010

    GE HC OEC 9900 Elite and GE OEC 9800 Fluoroscopes Snubber Boards are a PCB with a 70 amp fuse to provide fused protection of internal system components from the high voltage system components, such as the X-ray tube or High Voltage Transformer. System model number A349855, Snubber Board number 00-880405-03 rev 5. This product is used for image intensified fluoroscopic x-rays for interventional radiologic procedures.

    FDA Enforcement
    Class II ·Terminated·GE OEC Medical Systems, Inc·August 29, 2012