BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    XVbeam2000

    FDA 510(k)
    FDA Class 2 ·Dental

    Vu a-POD™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981041946·39x30mm Trial Rasp 14mm 8 deg

    OXYGEN DIVERTER VALVE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VERISUITE 1.8, VERISUITE-PARTICLE 1.8, VERISUITE, VERISUITE-PARTICLE

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD MICROFINE PLUS INSULIN SYRINGE

    FDA Adverse Event
    Injury ·BD MEDICAL - DIABETES CARE·Product code FMF·March 27, 2019

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·April 20, 2020

    CARPENTIER-EDWARDS PERIMOUNT MAGNA AORTIC BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·November 13, 2008

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 6, 2011

    GYNECARE PROLIFT TOTAL PELVIC FLOOR REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·July 18, 2013

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·April 20, 2020

    BD INTIMA-II CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FPA·June 16, 2020

    PEN NEEDLE 32X4 LA 5B

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·October 15, 2019