BEUDAMED
    7 results · 27ms · 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.
    Filters Regulation: Us FDA ×

    AESCULAP LAPAROSCOPES

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    GENTIAN VIOLET

    FDA 510(k)
    FDA Class 1 ·Hematology

    CALFORMA CALCIUM SULFATE BONE GRAFT BARRIER, MODEL 0.5G/1.0G

    FDA 510(k)
    FDA Class 2 ·Dental

    M2A-MAGNUM PF CUP 44ODX38ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·September 24, 2017

    PRIME 5TH WHEEL STRETCHER, 30"

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·February 4, 2013

    STAIR PRO - MODEL 6252

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FPP·December 10, 2010

    SENSOR ENLITE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·July 17, 2014