BEUDAMED
    26 results · 24ms · Sources: EU EUDAMED, US FDA

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    SYNTHES 1.5MM TI BROW LIFT SCREW

    FDA 510(k)
    FDA Class 2 ·Dental

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169328723·TEMPLATE 3002935 ZEVO 35MM 2 LVL

    RMO

    FDA UDI
    Rmo, Inc.·00885797100290·DUAL-TOP TAD SYSTEM KIT

    FacetFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361019831·Facet Screw, Cann, Gen 2, 4.5 x 35mm

    ACCESS TESTOSTERONE REAGENTS FOR USE ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 33560, 33565

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    KFA-63 KNEE AND FOOT ARRAY

    FDA 510(k)
    FDA Class 2 ·Radiology

    HEMOCUE GLUCOSE 201+ SYSTEM

    FDA Adverse Event
    Malfunction ·HEMOCUE AB·Product code CGA·July 18, 2017

    HEMOCUE GLUCOSE 201+ SYSTEM

    FDA Adverse Event
    Malfunction ·HEMOCUE AB·Product code CGA·July 18, 2017

    HEMOCUE GLUCOSE 201+ ANALYZER

    FDA Adverse Event
    Malfunction ·HEMOCUE AB·Product code LFR·May 23, 2011

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024

    GLUCOSE 201+ ANALYZER

    FDA Adverse Event
    Malfunction ·HEMOCUE AB·Product code CGA·February 26, 2015

    GLUCOSE 201+ ANALYZER

    FDA Adverse Event
    Malfunction ·HEMOCUE AB·Product code CGA·February 26, 2015

    GLUCOSE 201+ ANALYZER

    FDA Adverse Event
    Malfunction ·HEMOCUE AB·Product code CGA·February 26, 2015

    GLUCOSE 201+ ANALYZER

    FDA Adverse Event
    Malfunction ·HEMOCUE AB·Product code CGA·February 26, 2015

    GLUCOSE 201+ ANALYZER

    FDA Adverse Event
    Malfunction ·HEMOCUE AB·Product code CGA·February 26, 2015

    GLUCOSE 201+ ANALYZER

    FDA Adverse Event
    Malfunction ·HEMOCUE AB·Product code CGA·February 26, 2015

    GLUCOSE 201+ ANALYZER

    FDA Adverse Event
    Malfunction ·HEMOCUE AB·Product code CGA·February 26, 2015

    HEMOCUE GLUCOSE 201+ SYSTEM

    FDA Adverse Event
    Malfunction ·HEMOCUE AB·Product code LFR·August 18, 2014

    TROCHANTERIC NAIL KIT, TI GAMMA3 Ø10X170MM X 125°

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS-KIEL·Product code HSB·March 13, 2013

    TOTAL ASR ACET IMP SIZE 62

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.·Product code KWA·February 16, 2011