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

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    QUANTIEN Measurement System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    N/A

    FDA UDI
    DOMICO MED-DEVICE, LLC·00810050241564·PAD, TABLE, 1.25 X 26.00 X 78.00

    TIDI

    FDA UDI
    TIDI PRODUCTS, LLC·00618125173259·TIDI Table Pads Frosty 26in x 78in x 1.25in 1 p...

    MAQUET FLOW-I C20, MAQUET FLOW-I C30, MODEL 66 77 200, 66 77 30

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ALMA LASERS FAMILY OF THERMO-XEL HANDPIECES, PIXEL MODELS: 2940, 1060

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·January 13, 2022

    PHENOM

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·April 29, 2024

    PIPELINE

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·April 29, 2024

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·June 5, 2013

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·June 15, 2011

    ACCU-CHEK SPIRITI

    FDA Adverse Event
    Malfunction ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·September 18, 2008

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Malfunction ·ANGIOSCORE, INC·Product code LIT·November 18, 2015

    TRUETRACK

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·November 21, 2017

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·February 29, 2012

    MEDTRONIC LEAD

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DXY·October 9, 2025

    MEDTRONIC LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·October 9, 2025

    MEDTRONIC ICD

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·October 9, 2025

    CONTEGRA PULMONARY VALVED CONDUIT

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code MWH·July 29, 2021

    REFLEX CATHETER

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·April 29, 2024

    MARKSMAN

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·April 29, 2024