BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    COLORGENE DNA HYBRIDIZATION TEST CMV CONFIRMATION

    FDA 510(k)
    FDA Class 2 ·Microbiology

    BioHorizons Tapered Short Implants

    FDA 510(k)
    FDA Class 2 ·Dental

    CLEARLINK ANTIMICROBIAL LUER ACTIVATED DEVICE (LAD) AND EXTENSION SETS WITH THE CLEARLINK ANTIMICROBIAL LUER ACTIVATED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORPORATION·Product code FKX·June 13, 2014

    SETROX S 53

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code DTB·December 7, 2012

    RESTORE ADVANCED RECHARGEABLE

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·October 12, 2010

    ACHIEVE ADVANCE MAPPING CATHETER

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DRF·March 3, 2026