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

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    HEPAQUANT

    FDA 510(k)
    FDA Class 2 ·Hematology

    Mini Twin

    FDA UDI
    Rmo, Inc.·00885797674104·MBT MINI LP 018 HK/3 5-5 20EA

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M3848130110·Self-Drilling Screw - Ø1.5 mm x 3 mm

    Rampart-O

    FDA UDI
    SPINEOLOGY INC.·M7402813011·Rampart-O

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0130110·Segmental Rod Reducer, Slim, Assembly

    Additive Orthopaedics Patient Specific 3D Locking Lattice Plates

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPARTAN S3 FACET SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    PENUMBRA SYSTEM REPERFUSION CATHETER 032

    FDA Adverse Event
    Death ·PENUMBRA, INC.·Product code NRY·May 15, 2014

    REVO MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWP·October 31, 2012

    ADJ PIN COLLET 2.0-3.2MM

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·August 11, 2010