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

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    ALLRAP/SLIP-N-GRIP

    FDA 510(k)
    FDA Class 1 ·Dental

    HEALTH LINE INTERNATIONAL CORPORATIONS,S IV ADMINISTRATIVE SETS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MAGEC® Spinal Bracing and Distraction System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SHUNT SENSOR SYS500

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·June 23, 2014

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Injury ·ROCHE HEALTH SOLUTIONS, INC.·Product code LZG·February 6, 2013

    MESHGRAFT II DERMATOME WITH RATCHET

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GFD·December 16, 2010

    COULTER® ACT DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC·Product code GKZ·December 7, 2010

    MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·June 11, 2021

    DURAN ANCORE RING

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·August 12, 2021

    MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·October 26, 2021

    MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·May 28, 2022

    CG COMPOSITE RING

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·September 2, 2020

    DURAN ANCORE RING

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·September 2, 2020

    DURAN ANCORE RING

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·July 29, 2021

    MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·July 19, 2022