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

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    Filters Status: Malfunction ×

    J-TIP SYRINGE

    FDA Adverse Event
    Malfunction ·NATIONAL MEDICAL PRODUCTS, INC.·Product code KZE·January 5, 2012

    J TIP NEEDLE-FREE INJECTION SYSTEM WITH LUER ADAPTER

    FDA Adverse Event
    Malfunction ·NATIONAL MEDICAL PRODUCTS, INC.·Product code KZE·October 1, 2010

    J-TIP

    FDA Adverse Event
    Malfunction ·NATIONAL MEDICAL PRODUCTS, INC.·Product code KZE·August 21, 2025

    J-TIP SYRINGE

    FDA Adverse Event
    Malfunction ·NATIONAL MEDICAL PRODUCTS, INC.·Product code KZE·November 9, 2011

    J-TIP SYRINGE

    FDA Adverse Event
    Malfunction ·NATIONAL MEDICAL PRODUCTS, INC.·Product code KZE·September 19, 2012

    J-TIP NEEDLE FREE INJECTOR

    FDA Adverse Event
    Malfunction ·NATIONAL MEDICAL PRODUCTS INC.·Product code KZE·July 16, 2012

    J-TIP .25

    FDA Adverse Event
    Malfunction ·NATIONAL MEDICAL PRODUCTS, INC.·Product code KZE·December 3, 2024

    J-TIP

    FDA Adverse Event
    Malfunction ·NATIONAL MEDICAL PRODUCTS, INC.·Product code KZE·June 11, 2019

    J-TIP SYRINGE

    FDA Adverse Event
    Malfunction ·NATIONAL MEDICAL PRODUCTS, INC.·Product code KZE·November 20, 2013

    HEPARIN INFUSION LINE

    FDA Adverse Event
    Malfunction ·NATIONAL MEDICAL CARE, INC. - MEDICAL PRODUCTS DIV.·Product code FPB·January 8, 1993

    HEAVY-DUTY BACK TABLE COVER, 60 IN. X 90 IN. / 152 CM X 229 CM

    FDA Adverse Event
    Malfunction ·O&M HALYARD, INC.·Product code PUI·August 26, 2019

    COULTER ACT DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code GKZ·July 7, 2010

    TECNIS IOL

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code HQL·May 20, 2024

    COULTER ACT DIFF PAK

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GGK·April 26, 2011

    COULTER® 4C® PLUS CELL CONTROL

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JPK·October 12, 2010

    COULTER® LH 500 INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·June 8, 2011

    COULTER® LH 780 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·December 3, 2010

    COULTER LH 750 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code LOQ·February 8, 2011

    COULTER® LH 500 INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·February 23, 2011

    COULTER LH 750 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code LOQ·March 17, 2011