BEUDAMED
    31 results · 23ms · Sources: EU EUDAMED, US FDA

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    EZ-TRAVELER 2500 SERIES MANUAL WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040062562·Endoflex Reamers 25 mm

    Metal Custom Rx

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746103223·BRACKET LEWIS 018 4.5MM TQ=0 A=0 R=0 PROFILE=HP...

    ULTRA COMPACT WRIST BLOOD PRESSURE MONITOR WITH INTELLISENSE, MODEL HEM-630

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWDERED LATEX EXAM GLOVES, PINK, WITH/WITHOUT STRAWBERRY SCENT, PROTEIN LABELING

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Span-America

    FDA UDI
    SPAN-AMERICA MEDICAL SYSTEMS, INC.·H93300267100100·ZIMMER ABDUCTION PILLOW SMALL 6/CS

    Span-America

    FDA UDI
    SPAN-AMERICA MEDICAL SYSTEMS, INC.·H93300267100200·ZIMMER ABDUCTION PILLOW MD 6/CS

    Span-America

    FDA UDI
    SPAN-AMERICA MEDICAL SYSTEMS, INC.·H93300267100300·ZIMMER ABDUCTION PILLOW LG 6/

    LIGASURE ATLAS HANDSWITCHING 37 CM

    FDA Adverse Event
    Malfunction ·COVIDIEN LLC (SHANGHAI)·Product code GEI·February 13, 2013

    NA

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·February 9, 2011

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·February 26, 2008

    ELEVATOR #301

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·June 2, 2016

    ELEVATOR #301

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·June 2, 2016

    OPTIFLUX 180NR DIALYZER FINISHED ASSMBLY

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING PLANT·Product code KDI·July 21, 2018

    ELEVATOR #301

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·May 19, 2016

    ELEVATOR #301

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·June 2, 2016

    OPTIFLUX 180NRE DIALYZER FINISHED ASSMBLY

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING PLANT·Product code KDI·August 13, 2018

    OPTIFLUX 180NR DIALYZER FINISHED ASSMBLY

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING PLANT·Product code KDI·July 27, 2018

    ELEVATOR #301

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·June 2, 2016

    FEMORAL STEM PRESS-FIT COLLARLESS STEM CEMENTLESS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·February 2, 2023