BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    HIGH-PRESSURE CONNECTOR TUBE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIG/TDM A, B, C

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SURETEX LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    POLYSORB 4-0 VL 30 CV-23

    FDA Adverse Event
    Injury ·COVIDIEN , FORMERLY US SURGICAL·Product code KOG·June 2, 2014

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 9, 2013

    LIGASURE V 5 MM SEALER DIVIDER

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·November 15, 2010

    Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code: 8881200037

    FDA Enforcement
    Class II ·Completed·Cardinal Health 200, LLC·July 31, 2019

    TO GORE-TEX® STRETCH VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021

    GORE-TEX® STRETCH VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021

    Ortho Minor Pack, part number AMS3710(A

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017

    GORE-TEX® STRETCH VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021

    ID NOW COVID-19 2.0 TEST KIT 24T JAPAN

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QWR·November 21, 2024