BEUDAMED
    158 results · 68ms · Sources: EU EUDAMED, US FDA

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    CASTLE

    FDA Adverse Event
    Other ·MAQUET INC.·Product code FSY·March 20, 2009

    CASTLE

    FDA Adverse Event
    Other ·MAQUET INC. (F.K.A. GETINGEUSA)·Product code FSY·October 1, 2009

    630 PDT LASER

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

    TECNIS IOL 3 PIECES LENSE

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·April 9, 2021

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·April 9, 2021

    NEUTROGENA VISIBLY CLEAR LIGHT THERAPY ACNE MASK EU

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER INC.·Product code OLP·August 26, 2019

    MAXENON XI 300

    FDA Adverse Event
    Malfunction ·QED INC·Product code FST·June 4, 2014

    GALAXY G3 6MM X 15CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·September 25, 2019

    NEUTROGENA LIGHT THERAPY ACNE SPOT TREATMENT

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER INC·Product code OLP·January 14, 2020

    4K SYNERGYUHD4 C-MOUNT CAMERA HEAD, AUTO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GCJ·June 20, 2024

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·February 24, 2023

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·February 24, 2023

    ARM BOARD, IV, FLEXIBLE, 4" X 9", BLUE PURR, OUILOCK 

    FDA Adverse Event
    Malfunction ·ORTHO & SURGICAL PRODUCTS ENTERPRISES S.A.·Product code KMK·April 27, 2026

    ARM BOARD, IV, FLEXIBLE, 4" X 9", BLUE PURR, OUILOCK 

    FDA Adverse Event
    Malfunction ·ORTHO & SURGICAL PRODUCTS ENTERPRISES S.A.·Product code KMK·April 27, 2026

    ARM BOARD, IV, FLEXIBLE, 4" X 9", BLUE PURR, OUILOCK 

    FDA Adverse Event
    Malfunction ·ORTHO & SURGICAL PRODUCTS ENTERPRISES S.A.·Product code KMK·April 27, 2026

    ARM BOARD, IV, FLEXIBLE, 4" X 9", BLUE PURR, OUILOCK 

    FDA Adverse Event
    Malfunction ·ORTHO & SURGICAL PRODUCTS ENTERPRISES S.A.·Product code KMK·April 27, 2026

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·November 1, 2022

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO MANUFACTURING NETHERLANDS·Product code MFK·March 1, 2022

    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