BEUDAMED
    379 results · 57ms · Sources: EU EUDAMED, US FDA

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    COMFORT PRODUCTS, INC.

    FDA registration
    COMFORT PRODUCTS, INC.·1 product·🇺🇸 United States

    BOSTON SILVER TEE SHIRT

    FDA Adverse Event
    COMFORT PRODUCTS, INC..·Product code IPT·January 8, 2010

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO MANUFACTURING NETHERLANDS·Product code POE·May 6, 2025

    REFRESH CONTACTS, CONTACT LENS COMFORT DROPS

    FDA Adverse Event
    Malfunction ·ALLERGAN SALES, LLC·Product code LPN·October 18, 2019

    BAND AID PLASTIC COMFORT FLEX BANDAGES

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER INC·Product code KGX·November 7, 2022

    BAND AID PLASTIC COMFORT FLEX BANDAGES

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER INC·Product code KGX·November 7, 2022

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·May 6, 2025

    B.BRAUN

    FDA Adverse Event
    Malfunction ·B.BRAUN MELSUNGEN AG·Product code FRN·April 12, 2021

    COMFORTGEL FULL FACEMASK WITH HEADGEAR

    FDA Adverse Event
    Death ·RESPIRONICS, INC.·Product code BZD·July 7, 2010

    Luma Wrap Phototherapy Swaddler is designed to provide centered and comfortable boundaries as a benefit for restive babies in the Neonatal Intensive Care Unit.

    FDA Enforcement
    Class II ·Terminated·Beevers Manufacturing & Supply, Inc.·August 20, 2014

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 24, 2026

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·September 29, 2023

    BAND AID PLASTIC COMFORT FLEX BANDAGES

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER INC·Product code KGX·September 1, 2022

    BAND AID PLASTIC COMFORT FLEX BANDAGES

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER INC·Product code KGX·September 1, 2022

    ASKU

    FDA Adverse Event
    Malfunction ·ASKU·Product code FMI·November 19, 2022

    ENTERPRISE 9000

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH POLSKA SP. ZO.O.·Product code FSA·August 31, 2012

    LEAD MODEL 304

    FDA Adverse Event
    Injury ·HOUSTON·Product code LYJ·June 10, 2025

    CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH ¿ MEDIUM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·April 23, 2024

    ION

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code EOQ·April 14, 2025

    CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH ¿ MEDIUM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·July 24, 2022