BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    CLASSIC ECG/STIMULATING NO. 1700 SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    3M™ Unitek™

    FDA UDI
    3M COMPANY·30605861029033·3M™ Unitek™ Stainless Steel Permanent First Bic...

    VANISH VARNISH, 5% SODIUM FLUORIDE VARNISH, MODEL 12245, VANISH VARNISH, 5% FLUORIDE VARNISH, MODEL 12247

    FDA 510(k)
    FDA Class 2 ·Dental

    GLUCANPRO

    FDA 510(k)
    FDA Unclassified ·Unknown

    QUICKVUE AT-HOME OTC COVID-19 TEST

    FDA Adverse Event
    Malfunction ·QUIDEL CORPORATION·Product code QKP·March 1, 2023

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·June 27, 2014

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·January 7, 2013

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK MFG·Product code KWQ·October 28, 2010