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

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    UniStrip1 Generic Blood Glucose Test Strips

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741624300·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674162430060·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1624300·16mm H x 24mm W x 30mm L x 0 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L162430120·16mm H x 24mm W x 30mm L XLIF Trial 12 degree L...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X162430120·16mm H x 24mm W x 30mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X16243080·16mm H x 24mm W x 30mm L x 8 degrees XLIF

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138883·Broach, 30 X 26, 13mm Height 22° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138890·Broach, 30 X 26, 15mm Height 22° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138920·Broach, 30 X 26, 21mm Height 22° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138913·Broach, 30 X 26, 19mm Height 22° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138906·Broach, 30 X 26, 17mm Height 22° Hyperlordotic

    TYCO ELECTRONICS ELECTROCARDIOGRAPH (ECG) LEADWIRE SET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HEMOSIL PROTEIN C

    FDA 510(k)
    FDA Class 2 ·Hematology

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·August 8, 2016

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 24, 2025

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 23, 2014

    MD HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·April 26, 2022

    VERSA-DIAL 46X18X53 HUM HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·April 26, 2022