BEUDAMED
    331 results · 77ms · Sources: EU EUDAMED, US FDA

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    UTAH MEDICAL PRODUCTS, INC.

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS INC·Product code KNS·February 8, 2006

    UTAH MEDICAL PRODUCTS, INC

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC·Product code FOS·October 25, 2006

    INTRAN PLUS

    FDA Adverse Event
    Death ·UTAH MED PRODUCTS, INC.·Product code KXO·September 6, 1996

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·August 26, 2020

    DELTRAN PLUS NEEDLELESS ARTERIAL BLOOD COLLECTION SYSTEM

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC.·Product code DRS·August 18, 2015

    INTRAN PLUS IUP-400

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS INC.·Product code KXO·February 25, 2009

    DELTRAN IV PLUS

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC.·Product code DRS·January 26, 2010

    404TT

    FDA Adverse Event
    Other ·UTAH MEDICAL PRODUCTS, INC.·Product code HDB·March 5, 2010

    DELTRAN PLUS NEEDLELESS ARTERIAL BLOOD COLLECTION SYSTEM

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC.·Product code DRS·March 8, 2010

    UMBILI-CATH 3.5 FR

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC.·Product code FOS·June 7, 2010

    UMBILICAL CATHETER

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC.·Product code FOS·April 26, 2010

    INTRAN PLUS

    FDA Adverse Event
    Death ·UTAH MEDICAL PRODUCTS, INC.·Product code KXO·August 2, 1996

    INTRAN PLUS

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC.·Product code KXO·August 2, 1996

    UMBILI-CATH

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC.·Product code FOS·November 8, 2016

    UMBILI-CATH

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC.·Product code FOS·September 4, 2015

    UTAH MEDICAL UMBILI-CATH

    FDA Adverse Event
    Injury ·UTAH MEDICAL PRODUCTS, INC.·Product code FOS·August 10, 2015

    CRD-201

    FDA Adverse Event
    Other ·UTAH MEDICAL PRODUCTS, INC.·Product code HFW·February 25, 2004

    UMBILI-CATH

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS INC.·Product code FOS·October 26, 2017

    UTAHLOOP ELECTROSURGICAL ELECTRODE GUIDE

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC.·Product code GEI·April 12, 2021

    UTAHLOOP ELECTROSURGICAL ELECTRODE GUIDE

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC.·Product code GEI·April 12, 2021