BEUDAMED
    7 results · 20ms · 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 ×

    CDI(TM) H/S CUVETTE, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110904·TIP GUARDS VENTED ORANGE PACK OF 100

    TRAVELER, MOTORIZED THREE-WHEELED VEHICLE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    620 FLUOROSCOPIC TABLE, TILT OR POWER MEDICAL TAB

    FDA 510(k)
    FDA Class 2 ·Radiology

    PKS CUTTING FORCEPS

    FDA Adverse Event
    Malfunction ·GYRUS MEDICAL INC·Product code GEI·November 2, 2010

    DXTEND STAND PE CUP D42 +3MM

    FDA Adverse Event
    Injury ·DEPUY FRANCE S.A.S.-SAINT PRIEST 3003895575·Product code HSD·July 7, 2014

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·December 19, 2012