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

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    ENDOWRIST VESSEL SEALER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Gyrus ACMI

    FDA UDI
    Gyrus ACMI, LLC·00821925015517·HOUSE-TYPE SS WIRE LOOP .12 MM DIAMETER 5.25 MM...

    REPROCESSED ELECTROSURGICAL INSTRUMENT

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

    ENDOMETRIAL SAMPLING SYRINGE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·March 18, 2002

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·April 13, 2023

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·February 10, 2023

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·February 19, 2016

    SEDLINE KIT

    FDA Adverse Event
    Malfunction ·MASIMO - 40 PARKER·Product code MWI·January 8, 2017

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·May 16, 2023

    TUMESCENT INFILTRATION PUMP

    FDA Adverse Event
    Malfunction ·COVIDIEN-PLYMOUTH·Product code FRN·October 3, 2014

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 29, 2013

    SYNCHRON LX RHEUMATOID FACTOR (RF) REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code DHR·June 25, 2011