BEUDAMED
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    THE INSIDES COMPANY LIMITED

    FDA registration
    THE INSIDES COMPANY LIMITED·1 product·🇳🇿 New Zealand

    The Insides Neo

    FDA UDI
    THE INSIDES COMPANY LIMITED·09421905447195·The Insides Neo x1 Pouch

    The Insides Neo

    FDA UDI
    THE INSIDES COMPANY LIMITED·09421905447225·The Insides Neo x1 Pouch

    ESSURE

    FDA Adverse Event
    Malfunction ·BAYER PHARMA AG·Product code HHS·October 26, 2015

    LAP-BAND SYSTEM

    FDA Adverse Event
    Injury ·RESHAPE LIFESCIENCES·Product code LTI·August 17, 2022

    CORPECTOMY CAGE WITH SET SCREW; SIZE 13X16MM, 26-36MM, 0°, 0-20°

    FDA Adverse Event
    Injury ·K2M, INC.·Product code MQP·May 9, 2022

    640G INSULIN PUMP MMT-1712K

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 1, 2021

    SERFAS ENERGY SUPER 90-S

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GEI·February 12, 2013

    AVANTI + 5F STD W/GW

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DRE·December 20, 2016

    SI AVANTI+ 7F STD W/GW NO OBT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DRE·December 20, 2016

    AVANTI + 5F STD W/GW

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DRE·December 20, 2016

    SI AVANTI+ 6F STD W/GW NO OBT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DRE·December 20, 2016

    SI AVANTI+ 6F STD W/GW NO OBT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DRE·December 20, 2016

    SI AVANTI+ TRANSRAD KIT 11CM

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DRE·December 20, 2016

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·December 7, 2010

    670G INSULIN PUMP MMT-1780KL

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·July 15, 2021

    DATEX OHMEDA GAS MACHINE ANESTHESIA

    FDA Adverse Event
    Injury ·DATEX OHMEDA, INC.·Product code BSZ·July 5, 2016

    EVIS EXERA III BRONCHOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code EOQ·September 5, 2023

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS - HOUSTON·Product code LYJ·June 7, 2017

    ACUITY

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·July 6, 2012