BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    AIA-PACK CA 125

    FDA 510(k)
    FDA Class 2 ·Immunology

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 8, 2006

    Route 92 Medical Delivery Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXIS SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Radiology

    UNKNOWN_MEDICAL_PRODUCT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 5, 2013

    CAPSUREFIX NOVUS

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

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 7, 2014