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

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    DUPLOJECT (0.5/1.0 ML, 2.0 ML, 5.0 ML)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108970·ARBISSER ANTERIOR CHAMBER CANNULA 27GA

    ENDIUS TITLE 2 POLY AXIAL SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BioStamp nPoint

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CAPIOX HEMOCONCENTRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDO·June 12, 1997

    FLEXOR RAABE GUIDING SHEATH

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·February 15, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER-SILICON VALLEY·Product code GEX·January 19, 2011

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 1, 2014