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

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    S-ROM LF FEMORAL HEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Accu-Beam

    FDA UDI
    TRANSAMERICAN TECHNOLOGIES INTERNATIONAL·B1779203170·Re-usable fiberoptic handpiece for lasers. 17ga...

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110928·STERILIZING CASE SINGLE VR

    NON-STERILE POWDER FREE GREEN BARRIER-PRO SYNTHETIC BUTADIENE COPOLYMER EXAMINATION GLOVE, COLOR: BLUE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PuraPly Micronized Wound Matrix (PuraPly MZ)

    FDA 510(k)
    FDA Unclassified ·Unknown

    DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 16, 2015

    BONE CEMENT

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC·Product code NDN·December 10, 2010

    BATTERY 14.8V, 6.3 AH LI-ION BATTERU

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 17, 2012