BEUDAMED
    21 results · 53ms · Sources: EU EUDAMED, US FDA

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    INVISION-PLUS NEURTAL

    FDA Adverse Event
    Other ·RYMED TECHNOLOGIES, INC.·Product code FPA·November 9, 2010

    INVISION-PLUS NEUTRAL DISPLACEMENT I.V. CONNECTOR

    FDA Adverse Event
    RYMED TECHNOLOGIES, INC.·Product code FPA·June 15, 2005

    RYMED CAP

    FDA Adverse Event
    Other ·RYMED TECHNOLOGIES INC·Product code FPA·March 7, 2014

    INVISION-PLUS NEUTRAL CAP

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC.·Product code FPA·November 22, 2010

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    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC·Product code FPA·December 17, 2010

    INVISION PLUS

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC.·Product code FPA·March 12, 2007

    INVISION PLUS

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC.·Product code FPA·January 17, 2007

    INVISION PLUS

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC.·Product code FPA·October 10, 2006

    INVISION PLUS

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC.·Product code FPA·November 30, 2006

    INVISION PLUS

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC.·Product code FPA·October 10, 2006

    INVISION PLUS NEUTRAL IV CONNECTOR

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC.·Product code FPA·December 7, 2007

    INVISION PLUS NEUTRAL IV CONNECTOR SYSTEM

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC.·Product code FPA·June 20, 2006

    INVISION-PLUS NEUTRAL IV CONNECTOR SYSTEM

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC·Product code FPA·June 20, 2006

    INVISION-PLUS JUNIOR

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC.·Product code FPA·July 7, 2009

    RYM-5001

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC.·Product code FPA·May 1, 2008

    INVISION PLUS / RYM 5000

    FDA Adverse Event
    Injury ·RYMED TECHNOLOGIES, INC.·Product code LHI·February 12, 2020

    INVISION PLUS

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC.·Product code FPA·August 10, 2006

    INVISION-PLUS WITH NEUTRAL ADV.

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, INC.·Product code FPA·April 10, 2015

    RYM-5000 InVision-Plus NEUTRAL I.V. Connector, packaged 200 units per box, 5 boxes per case (1000 units/case); labeled as Sterile-Nonpyrogenic; assembled in Mexico for Rymed Technologies, Inc., Austin, TX.

    FDA Recall
    Terminated ·Rymed Technologies, Inc.·Product code FPA·May 25, 2006

    RYM-5000 InVision-Plus Neutral Displacement I.V. Connector, packaged 200 units per box, 5 boxes per case (1000 units/case); labeled as Sterile-Nonpyrogenic; assembled in Mexico for Rymed Technologies, Inc., Austin, TX.

    FDA Recall
    Terminated ·Rymed Technologies, Inc.·Product code FPA·May 25, 2006