BEUDAMED
    17 results · 29ms · Sources: EU EUDAMED, US FDA

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    Neurosoft TMS

    FDA 510(k)
    FDA Class 2 ·Neurology

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694036009·3.0/4.0mm Solid Headless Driver, Tapered

    Rumex

    FDA UDI
    RUMEX INTERNATIONAL CORP.·00840159905500·Corneal Trephine Blades, 8.50 mm, Stainless Steel

    BONASTENT® Tracheal/Bronchial

    FDA UDI
    Sewoon Medical Co., Ltd.·08806369468848·

    B-P TOTAL HIP SYSTEM

    FDA UDI
    ENDOTEC, INC.·00814193024046·B-P MODULAR EXTENSION W/ULTRACOAT - 9 MM X 75 MM

    K162309

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code PGW·November 14, 2019

    FOB ONE STEP RAPID TEST

    FDA 510(k)
    FDA Class 2 ·Hematology

    AUTOCAT INTRA-AORTIC BALLOON PUMP SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FRAME 9733886 SMALL ACTIVE HC

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 1, 2019

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·October 6, 2017

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 10, 2013

    GENEXPERT SOFTWARE

    FDA Adverse Event
    Malfunction ·CEPHEID·Product code OQW·April 28, 2011

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 16, 2008

    TALENT AAA STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·March 13, 2017

    ENDURANT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·March 13, 2017

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 3/26MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 14, 2023

    VENTED AUTOFEED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·October 19, 2016