BEUDAMED
    1,597 results · 33ms · Sources: EU EUDAMED, US FDA

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    ARROW CVC SET: 3-LUMEN 12 FR X 16 CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DQY·June 16, 2020

    PALINDROME SAPPHIRE 23/40KT VT

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code MPB·October 16, 2008

    BIOPATCH

    FDA Adverse Event
    Injury ·ETHICON·Product code FRO·October 31, 2012

    IMPLANTED PORT WITH GROSHONG CATH

    FDA Adverse Event
    Injury ·BARD·Product code LJS·July 13, 2015

    VANTEX TLC

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES INC·Product code GBP·May 21, 2025

    ARROW PI JACC KIT: 3L 6 FR X 25 CM CG+

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL LLC·Product code LJS·July 7, 2025

    BARD POWER PICC 3L CATHETER

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS·Product code LJS·November 3, 2017

    ARROW MULTILUMEN/PSI KIT 9 FR X 11.5 CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL LLC·Product code FOZ·October 11, 2023

    BIOPATCH 4150

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES PR·Product code FRO·December 18, 2012

    CORDIS INTRODUCER

    FDA Adverse Event
    Injury ·ARROW·Product code DYB·June 6, 2007

    PALINDROME HSI KIT 23/40 CM X5

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code MSD·July 10, 2012

    ARROW MULTILUMEN/PSI KIT 9 FR X 11.5 CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL LLC·Product code FOZ·October 11, 2023

    ARROW MULTILUMEN/PSI KIT 9 FR X 11.5 CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL LLC·Product code FOZ·October 11, 2023

    MCGAW, INC.

    FDA Adverse Event
    Other ·MCGAW, INC.·Product code FPB·August 15, 1997

    HERCEPTEST KIT

    FDA Adverse Event
    Malfunction ·DAKO CORP.·Product code LIJ·December 3, 1998

    PALINDROME SAPPHIRE 28/45SP VT

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code MPB·March 9, 2009

    MAXCORE

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·December 8, 2025

    UNKNOWN OXFORD BEARING

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·August 7, 2025

    MOSAIC MITRAL BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·August 7, 2014

    ECHELON

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. D/B/A EV3 NEUROVASCULAR·Product code KRA·August 11, 2022