BEUDAMED
    18 results · 28ms · Sources: EU EUDAMED, US FDA

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    Remvia, LLC

    FDA registration
    Remvia, LLC·2 products·🇺🇸 United States

    Remvia NightGuard

    FDA 510(k)
    FDA Unclassified ·Unknown

    PREMVIA

    FDA 510(k)
    FDA Unclassified ·Unknown

    emVia Lancing Device

    Device
    EU MDR · Eu Md Class 1 ·i-SENS, Inc.·On the market

    HILL-ROM VIA STRETCHER (P1300 - P1303)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SR90D RATCHING CAP REMV/I

    FDA Adverse Event
    Injury ·STRYKER SPINE BORDEAUX·Product code LXH·November 21, 2012

    EPIC? VASCULAR

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIO·June 30, 2014

    EPIC?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIO·June 30, 2014

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·December 20, 2012

    OXYGENATOR

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·August 10, 2020

    HLM TUBING SETW/BIOLINE COATING

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·August 21, 2020

    ENDURANT II ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·December 20, 2012

    VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.

    FDA Enforcement
    Class III ·Terminated·MICROVENTION INC.·June 16, 2021

    VIA Microcatheter VIA 27 REF VIA-27-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.

    FDA Enforcement
    Class III ·Terminated·MICROVENTION INC.·June 16, 2021

    VIA Microcatheter VIA 17 REF VIA-17-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.

    FDA Enforcement
    Class III ·Terminated·MICROVENTION INC.·June 16, 2021

    VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.

    FDA Recall
    Terminated ·MICROVENTION INC.·Product code DQY·April 21, 2021

    VIA Microcatheter VIA 17 REF VIA-17-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.

    FDA Recall
    Terminated ·MICROVENTION INC.·Product code DQY·April 21, 2021

    VIA Microcatheter VIA 27 REF VIA-27-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.

    FDA Recall
    Terminated ·MICROVENTION INC.·Product code DQY·April 21, 2021