BEUDAMED
    446 results · 132ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    TERUMO MEDICAL CORP.

    FDA Adverse Event
    Malfunction ·TERUMO (PHILIPPINES) CORP.·Product code FMI·October 27, 2017

    ANGIO-SEAL

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code MGB·February 25, 2026

    TERUMO SAMPLING SITE COUPLER

    FDA Adverse Event
    Malfunction ·TERMUO MEDICAL CORP.·Product code BRZ·January 28, 2005

    HYPODERMIC NEEDLE-PRO SYRINGE AND NEEDLE WITH NEEDLE PROTECT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMI·July 22, 2005

    HYPODERMIC NEEDLE-PRO SYRINGE AND NEEDLE WITH NEEDLE PROTECT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMI·November 19, 2004

    HYPODERMIC NEEDLE-PRO SYRINGE AND NEEDLE WITH NEEDLE PROTECT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMI·January 19, 2007

    HYPODERMIC NEEDLE-PRO & NEEDLE WITH NEEDLE PROTECTION DEVICE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMI·December 27, 2006

    HYPODERMIC NEEDLE-PRO AND NEEDLE WITH NEEDLE PROTECTION DEVICE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMI·December 5, 2007

    HYPODERMIC NEEDLE-PRO AND NEEDLE WITH NEEDLE PROTECTION DEV

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMI·August 4, 2006

    HYPODERMIC NEEDLE-PRO SYRINGE AND NEEDLE WITH NEEDLE PROTECT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMI·August 4, 2006

    SURFLO IV CATHETER

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORP.·Product code FOZ·September 30, 2015

    RADIFOCUS INTRODUCER KIT

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORP.·Product code DYB·February 4, 2009

    PINNACLE DESTINATION RENAL GUIDING SHEATH

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORP.·Product code DYB·January 9, 2009

    PINNACLE R/O II INTRODUCER KIT

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORP.·Product code DYB·February 3, 2010

    PINNACLE DESTINATION RENAL GUIDING SHEATH

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORP.·Product code DYB·March 18, 2010

    PINNACLE SHEATH

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORP.·Product code DYB·June 8, 2010

    SUREFLO INJECTION PLUG

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORP.·Product code FOZ·August 28, 1996

    SURFLO INJECTION PLUG

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORP.·Product code FOZ·August 28, 1996

    VENOJECT II SODIUM FLUORIDE TUBE

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORP.·Product code JKA·September 6, 1996

    SURFLO INJECTION PLUG

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORP.·Product code FOZ·August 28, 1996