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

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    MICRO CAUTERY NEEDLES

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

    discovery®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011891400000·1 case discovery® pearl+smart McLaugh. 22 / Bra...

    MODIFICATION TO AVIE A1C TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    Voyager Trajectory Array Guide (V-TAG)

    FDA 510(k)
    FDA Class 2 ·Neurology

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 6, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 7, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 6, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·April 27, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·April 16, 2018

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 24, 2014

    RADIAL JAW 3 BIOPSY FORCEPS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA·Product code FCL·November 4, 2010

    VASOVIEW 6 EVH SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·December 26, 2012

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 5, 2018

    ZERO-P VA IMPLANT 7MM HEIGHT LORDOTIC-STERILE

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code OVE·October 1, 2018

    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