BEUDAMED
    32 results · 24ms · Sources: EU EUDAMED, US FDA

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    X10 HEADSET WITH X-SERIES BASIC SOFTWARE, X24 HEADSET WITH X-SERIES BASIC SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Neurology

    ArgenIS

    FDA UDI
    ARGEN CORPORATION, THE·D818131383·MUA AO RP 2.5GH Str

    ZIRPRIME

    FDA 510(k)
    FDA Class 2 ·Dental

    MODEL 780

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123322·15mm Broach, 38 x 30, 12° Lordosis

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123384·21mm Broach, 38 x 30, 12° Lordosis

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123353·18mm Broach, 38 x 30, 12° Lordosis

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123285·11mm Broach, 38 x 30, 12° Lordosis

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123315·14mm Broach, 38 x 30, 12° Lordosis

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123346·17mm Broach, 38 x 30, 12° Lordosis

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123339·16mm Broach, 38 x 30, 12° Lordosis

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123360·19mm Broach, 38 x 30, 12° Lordosis

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123292·12mm Broach, 38 x 30, 12° Lordosis

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123308·13mm Broach, 38 x 30, 12° Lordosis

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123377·20mm Broach, 38 x 30, 12° Lordosis

    PROPHECY INFINITY

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HSN·March 29, 2021

    APPOSE ULC 35 WIDE SKIN STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY NELLCOR·Product code GDT·May 13, 2013

    CAPSUREFIX NOVUS MRI

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code NVN·June 16, 2011

    IRR FCP BAY BIP 8 3/4 1.0

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GEI·August 12, 2008

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 8, 2016