BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    Biomet Variable Pitch Compression Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BAROUK SCREW - 3 0MM X 32MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HWC·April 7, 2020

    VIVID POST TRANSLUCENT

    FDA UDI
    BIOLOREN SRL·08056099233272·Cylindrical fiberglass light transmitting posts...

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319720967·Gillies-Sheehan Needle Holder w/ Scissors 6-1/2...

    Medallion®

    FDA UDI
    Merit Medical Systems, Inc.·00884450146279·

    VDRL ANTIGEN WITH BUFFERED SALINE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code GMT·November 9, 2012

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    STELLAR 404T

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 5, 2024

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·October 10, 2014

    OXFORD UNICOMPARTMENTAL KNEE RIGHT MEDIAL TIBIAL TRAY SIZE D

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·July 13, 2011

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·June 10, 2013