BEUDAMED
    42 results · 25ms · Sources: EU EUDAMED, US FDA

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    BD Y SITE ASSEMBLY

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·June 26, 2023

    ASSEMBLY NAC Y-SITE (0.104 POCKET) OEM

    FDA Adverse Event
    Malfunction ·Product code FPA·July 17, 2021

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 26, 2013

    RESTORE SENSOR MRI

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 18, 2014

    HC234 CPAP HUMIDIFIER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·May 24, 2011

    COBAS 4800 HPV TEST, CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MAQ·December 22, 2011

    COBAS 4800 HPV TEST, CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MAQ·May 23, 2013

    DELTA TT PRO

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A·Product code LPH·January 2, 2026

    COBAS 4800 HPV TEST, CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MAQ·May 10, 2012

    TT AUGMENTED 360 BASEPLATE #S-R 15°

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code PHX·January 3, 2024

    SMR CEMENTLESS FINNED STEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code HSD·November 14, 2023

    COBAS 4800 HPV TEST

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS·Product code MAQ·July 17, 2017

    THV 1000-29 3F AORTIC BIO 29MM

    FDA Adverse Event
    Injury ·MEDTRONIC 3F THERAPEUTICS, INC.·Product code LWR·August 8, 2024

    THV 1000-29 3F AORTIC BIO 29MM

    FDA Adverse Event
    Malfunction ·MEDTRONIC 3F THERAPEUTICS, INC.·Product code LWR·December 5, 2025

    THV 1000-29 3F AORTIC BIO 29MM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·November 25, 2025

    THV 1000-29 3F AORTIC BIO 29MM

    FDA Adverse Event
    Injury ·MEDTRONIC ATS 3F THERAPEUTICS·Product code LWR·February 10, 2014

    THV 1000-29 3F AORTIC BIO 29MM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·December 9, 2018

    THV 1000-29 3F AORTIC BIO 29MM

    FDA Adverse Event
    Injury ·MEDTRONIC 3F THERAPEUTICS, INC.·Product code LWR·June 5, 2024

    THV 1000-29 3F AORTIC BIO 29MM

    FDA Adverse Event
    Injury ·MEDTRONIC 3F THERAPEUTICS, INC.·Product code LWR·June 17, 2024

    THV 1000-29 3F AORTIC BIO 29MM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·October 21, 2021