BEUDAMED
    10,000 results · 65ms · 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 ×

    JACK SCALER

    FDA Adverse Event
    Malfunction ·PDT, INC.·Product code EMN·February 3, 2020

    PHOTOFRIN 630 PDT LASER

    FDA Adverse Event
    Injury ·PINNACLE BIOLOGICS INC.·Product code MVF·January 6, 2017

    PERC TRACH TUBE

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code BTO·August 23, 2006

    PERC TRACH TUBE

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code BTO·August 23, 2006

    630 PDT LASER

    FDA Adverse Event
    Injury ·PINNACLE BIOLOGICS, INC.·Product code MVF·March 11, 2021

    AMPLATZER DUCT OCCLUDER II

    FDA Adverse Event
    Death ·AGA MEDICAL CORPORATION·Product code MAE·December 27, 2017

    DIOMED

    FDA Adverse Event
    Injury ·DIOMED INC.·Product code GEX·July 26, 2001

    PHOTOFRIN 630 PDT LASER

    FDA Adverse Event
    Injury ·PINNACLE BIOLOGICS INC·Product code MVF·January 18, 2017

    OPTIGUIDE® DCYL CYLINDRICAL DIFFUSER

    FDA Adverse Event
    Malfunction ·PINNACLE BIOLOGICS, INC.·Product code MVG·April 15, 2025

    UNSPECIFIED TRACHEAL TUBE

    FDA Adverse Event
    Injury ·MALLINCKRODT MEDICAL·Product code BTR·October 21, 2025

    DEXCOM G7

    FDA Adverse Event
    Injury ·DEXCOM, INC.·Product code QBJ·July 7, 2025

    630 PDT LASER

    FDA Adverse Event
    Injury ·PINNACLE BIOLOGICS, INC.·Product code MVF·March 11, 2021

    630 PDT LASER

    FDA Adverse Event
    Injury ·PINNACLE BIOLOGICS, INC.·Product code MVF·March 11, 2021

    OPTIGUIDE FIBER OPTIC DIFFUSER

    FDA Adverse Event
    Injury ·PINNACLE BIOLOGICS INC·Product code MVG·November 1, 2024

    630 PDT LASER

    FDA Adverse Event
    Injury ·PINNACLE BIOLOGICS INC·Product code MVF·November 1, 2024

    PDT

    FDA Adverse Event
    DUSA·Product code MVF·October 24, 2017

    BD PYXIS¿ ES SERVER

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·May 6, 2026

    LASERSCOPE

    FDA Adverse Event
    Malfunction ·LASERSCOPE·Product code GEX·March 20, 2003

    OES BRONCHOFIBERSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code EOQ·December 12, 2019

    AVEA II VENTILATOR

    FDA Adverse Event
    Malfunction ·VYAIRE MEDICAL·Product code CBK·April 5, 2022