BEUDAMED
    19 results · 31ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    GALLANT HF

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NIK·April 17, 2021

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVN·April 17, 2021

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVY·April 17, 2021

    RICHARD ALLAN SURGICAL NEEDLE

    FDA Adverse Event
    Malfunction ·ASPEN SURGICAL PRODUCTS, INC.·Product code GAB·November 20, 2012

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORS

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·April 1, 2014

    OCTRODE LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·July 6, 2022

    SAFIL VIOLET 3/0(2)8X45CM HR26 TO (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·March 11, 2016

    PENTA

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 28, 2014

    ASSURITY MRI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·July 18, 2022

    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 7, 2022

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVN·July 18, 2022

    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·December 5, 2022

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVY·February 28, 2025

    OMNISTEM "DEVICE #1"

    FDA Adverse Event
    Injury ·PHYSIO-TECHNOLOGY·Product code GZC·August 22, 1997

    INVERNESS EAR PIERCING SYSTEM

    FDA Adverse Event
    Other ·INVERNESS CORP.·Product code JYS·February 8, 2001

    SENSICARE NONLATEX EXAMINATION GLOVES

    FDA Adverse Event
    Other ·MAXXIM MEDICAL CANADA, LTD.·Product code LYZ·March 18, 1999

    UNKNOWN SALINE IMPLANTS

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·February 28, 2024

    CONTACT DETACH

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·October 27, 2025

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·July 16, 2019