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

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    Genesys Spine Binary Lumbar Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Dandy Clear Aligners

    FDA UDI
    Orthly, Inc.·00860006891206·

    DD cubeX2 HS

    FDA 510(k)
    FDA Class 2 ·Dental

    OSTEOMED SMARTFLEX CRANIAL SPRING DISTRACTOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·January 4, 2023

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 7, 2025

    QUADRA ASSURA CRT-D, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·October 15, 2014

    ADVANTAGE FIT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 17, 2013

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 24, 2011

    BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·May 16, 2023

    BINAXNOW COVID-19 AG CARD

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 2, 2022