BEUDAMED
    13 results · 20ms · Sources: EU EUDAMED, US FDA

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    chromID MRSA

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ProLift

    FDA UDI
    Life Spine, Inc.·00190837200312·

    FOR PLAY, SLIP, PREPAIR - PERSONAL LUBRICANTS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    EMM SURGICAL DRAPE-SPUNLACE W/PE SIDES, MODEL 13-004

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BD ANGIOCATH¿ IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·December 19, 2017

    PULSE GEN MODEL 102R

    FDA Adverse Event
    Death ·CYBERONICS, INC.·Product code LYJ·October 8, 2014

    FLEXTEND

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 6, 2011

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 7, 2013

    BD ANGIOCATH IV CATHETER 20GA 1.88IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·June 24, 2020

    BD INSYTE¿ PERIPHERAL VENOUS CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FOZ·March 20, 2018

    12-Panel Dip Drug Screen with adulterant, Item No. PSDA-12BUP, PSD-6MTDBO300, PSD-10PPX, PSD-10MOX, 60960D, 61127D, DCC-81205-5, IMCA-10M5.

    FDA Enforcement
    Class III ·Terminated·Ameditech Inc·December 30, 2015

    Integrity 1.1. Integrity is the interface and control software for the Elekta range of medical digital linear accelerators and is intended to assist a licensed practitioner in the delivery of radiation to defined target volumes.

    FDA Enforcement
    Class II ·Terminated·Elekta, Inc.·April 9, 2014

    Medical Linear Accelerator

    FDA Enforcement
    Class II ·Terminated·Elekta, Inc.·September 14, 2016