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

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    DEROYAL STERILE NEONATAL BLOOD PRESSURE CUFF

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VENTRALIGHT

    FDA UDI
    Davol Inc.·00801741131011·Ventralight ST Mesh with Echo 2 Positioning Sys...

    NONE

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code UNK·December 11, 2009

    HOLLISTER KARAYA PASTE

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    KinematX Total Wrist Arthroplasty System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TENOR SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code KWQ·December 11, 2009

    COBAS INTEGRA D-DIMER

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GHH·March 6, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    KAPPA 700 D

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NVZ·August 8, 2014