BEUDAMED
    13 results · 23ms · Sources: EU EUDAMED, US FDA

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    H.A.M. APPLICATOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    ASAHI PRECIOUS GUIDE CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Dynamika

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD MULTI-CHECK¿

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·May 5, 2023

    BD MULTI-CHECK¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 22, 2023

    BD MULTI-CHECK¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 22, 2023

    PROXIMATE I L S INTRALUMINAL STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.·Product code GAG·September 13, 1996

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·February 14, 2013

    SOLETRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·December 27, 2010

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·July 28, 2014

    Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000

    FDA Enforcement
    Class II ·Terminated·Intersurgical Inc·July 4, 2018

    COMMANDER DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code NPT·May 19, 2023

    BD MULTI-CHECK¿

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·July 26, 2023