BEUDAMED
    5,401 results · 36ms · Sources: EU EUDAMED, US FDA

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    PLEXA PROMRI S DX 65/15

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVY·October 6, 2024

    TEO DR

    FDA Adverse Event
    Malfunction ·MICROPORT CRM S.R.L.·Product code LWP·September 26, 2022

    V-GO DISPOSABLE INSULIN DELIVERY DEVICE

    FDA Adverse Event
    Injury ·ZEALAND PHARMA U.S. INC.·Product code LZG·September 7, 2021

    PRECISETYPE HEA MOLECULAR BEADCHIP KIT

    FDA Adverse Event
    Malfunction ·BIOARRAY SOLUTIONS, LIMITED·Product code PEP·May 18, 2023

    TRANSVENE

    FDA Adverse Event
    Injury ·MEDTRONIC INC., CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·January 9, 2004

    TRANSVENE

    FDA Adverse Event
    Injury ·MEDTRONIC INC., CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 10, 2005

    2649622-1999-00498

    FDA Adverse Event
    Malfunction ·November 12, 1999

    V-GO DISPOSABLE INSULIN DELIVERY DEVICE

    FDA Adverse Event
    Injury ·VALERITAS, INC.·Product code LZG·June 1, 2018

    MEDTRONIC

    FDA Adverse Event
    Injury ·MEDTRONIC INC.·Product code DTB·August 13, 2001

    DEFIBRILLATOR/MONITOR/PACEMAKER

    FDA Adverse Event
    Injury ·ZOLL MEDICAL CORP.·Product code LDD·June 17, 1994

    DEFIBRILLATOR/MONITOR/PACEMAKER

    FDA Adverse Event
    Injury ·ZOLL MEDICAL CORP.·Product code LDD·June 17, 1994

    GEM II DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·March 13, 2000

    HEA 1.2 BEADCHIP KIT, SLIDE

    FDA Adverse Event
    Malfunction ·BIOARRAY SOLUTIONS LTD.·Product code PEP·August 4, 2017

    GUIDANT

    FDA Adverse Event
    Injury ·GUIDANT CORP·Product code LWS·November 15, 2004

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC INC., CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 10, 2003

    OVATIO

    FDA Adverse Event
    Injury ·SORIN CRM·Product code MRM·August 23, 2013

    U.S. SURGICAL

    FDA Adverse Event
    U.S. SURGICAL·Product code GAO·April 10, 2003

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·July 10, 2002

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 2002

    GEM DR

    FDA Adverse Event
    Injury ·MEDTRONIC INC., CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 10, 2002