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

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    REMSTAR SE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HEX-FIX

    FDA UDI
    Smith & Nephew, Inc.·03596010069870·STAINLESS STEEL HALF PIN 6MM X 60MM

    ArgenZ HT+ 95x20 OM2

    FDA UDI
    ARGEN CORPORATION, THE·D818122769·Dental porcelain/ceramic restoration kit

    LIFESCAN ONETOUCH ULTRA CONTROL SOLUTION

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    NEODENT IMPLANT FOR ORTHODONTIC ANCHORAGE

    FDA 510(k)
    FDA Class 2 ·Dental

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·September 30, 2019

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·September 30, 2019

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·September 30, 2019

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·September 30, 2019

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·January 15, 2020

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·September 5, 2019

    24G X 0.75IN (0.7 X 19 MM) INSYTE AUTOGUARD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·September 27, 2019

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·May 21, 2013

    DIMENSION EXL WITH LM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·September 26, 2014

    ASR ACETABULAR IMPLANT SIZE 50

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·June 3, 2011

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·May 12, 2017

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·August 25, 2017

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·September 27, 2019

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·September 27, 2019

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·August 8, 2017