BEUDAMED
    30 results · 28ms · Sources: EU EUDAMED, US FDA

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    SINGLE USE GROUNDING PAD

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    NexxZr™ T / D-100-16-NT-C400-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271113467·

    VESSEL GUARDIAN

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    WIROBOND C

    FDA 510(k)
    FDA Class 2 ·Dental

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 16, 2021

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 31, 2023

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 15, 2022

    MPACT ACETABULAR SHELL Ø 60 TWO-HOLES

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·April 27, 2016

    OPTEASE RETRIEVABLE VENA CAVA FILTER - 55CM-EU

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DTK·May 29, 2013

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·June 17, 2011

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·August 22, 2008

    BD INSYTE AUTOGUARD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·July 29, 2024

    LACTATE DEHYDROGENASE

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code CFG·June 11, 2020

    MEDTRONIC LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·October 8, 2021

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 5, 2019

    LACTATE DEHYDROGENASE

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES (IRVING IA/CC)·Product code CFG·February 25, 2020

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 5, 2019

    UNKNOWN KNEE TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 10, 2019

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 5, 2019

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 5, 2019