BEUDAMED
    58 results · 25ms · Sources: EU EUDAMED, US FDA

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    INJECTION PIPETTE; HOLDING PIPETTE; BIOPSY PIPETTE; DENUDING PIPETTE; PARTIAL ZONA DISSECTION (PZD) PIPETTE; ASSISTED HA

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

    Synergy

    FDA UDI
    Rmo, Inc.·00885797101037·ROTH SY 022 HK MAX/3 5-5 20EA

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540134370·DISIMPACTION FCPS., RIGHT

    ROTA-TRACH TRACHEOSTOMY TUBE MODEL ROTA-TRACH

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VANGUARD REPROCESSED INFLATION DEVICES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 17, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·October 7, 2020

    LIGASURE

    FDA Adverse Event
    Injury ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·July 21, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 20, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 26, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 9, 2021

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 2, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 13, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 16, 2019

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·April 24, 2020

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·March 14, 2019

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 16, 2021

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·May 2, 2013

    T-LINK DATA MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEM CORP.·Product code DWA·May 20, 2011

    PULSE GEN MODEL UNKNOWN

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·August 8, 2008