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

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    LoFric Elle

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    VITA TITANKERAMIK

    FDA UDI
    Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft·J017B2112120·VITA TITANKERAMIK INTENSIVE, IN2, 12 g

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327090376·2.0 MP LE FORT I PLATE,12MM ADV.,L

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0112120·Tap, Cannulated, 8.5 mm

    InSePtion MIS Fixation System

    FDA UDI
    Kalitec Direct LLC·B07314K0112120·Rasp, 12 and 14mm

    FILTERFLO H

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SMR SHOULDER SYSTEM- REVISION STEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523183807·2 Hole, 12 mm, Right, 1-Level Anterior Cervical...

    A Plus

    FDA UDI
    A PLUS INTERNATIONAL INC.·00683534840245·Sterile Lap Sponges , 12"X12", Prewashed, Plast...

    A Plus

    FDA UDI
    A PLUS INTERNATIONAL INC.·00683534840375·12"X12", Unwashed, Bleached White, 5 Pc(s)/Pack...

    A Plus

    FDA UDI
    A PLUS INTERNATIONAL INC.·00683534840368·12"X12", Prewashed, Bleached White, 5 Pc(s)/Pac...

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OYC·May 17, 2018

    SURESTEP

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CGA·April 23, 2001

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·January 10, 2023

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·January 9, 2023

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·February 11, 2021

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 10, 2015

    CELL-DYN 1800 ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·October 28, 2008

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·July 12, 2011

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·July 8, 2013