BEUDAMED
    21 results · 71ms · Sources: EU EUDAMED, US FDA

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    THE BODY DOCTOR LTD

    FDA registration
    THE BODY DOCTOR LTD·2 products·🇬🇧 United Kingdom

    MEDICAL ACTION INDUSTIRES

    FDA Adverse Event
    Malfunction ·JIANGSU PROVINCE JIANERKANG MEDICAL DRESSING CO.,·Product code GDY·May 30, 2017

    SINGLE USE 8MM PIERCER PROBE - STERILE

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDX·October 29, 2018

    GEN CASEFRAME NON OPTICAL 115V

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code JDX·October 29, 2018

    DOLLAR GENERAL EFFERVESCENT DENTURE CLEANSER

    FDA Adverse Event
    Injury ·TOWER LABORATORIES, LTD.·Product code EFT·December 11, 2008

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·May 16, 2018

    ZILVER PTX 35 DRUG-ELUTING STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·March 7, 2019

    ECHOTIP PROCORE ENDOBRONCHIAL HD BIOPSY NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·May 25, 2017

    G7 HI-WALL E1 LINER 32MM C

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code PBI·September 4, 2020

    G7 PPS LTD ACET SHELL 48C

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code PBI·September 4, 2020

    CURE CATHETER

    FDA Adverse Event
    Malfunction ·INTEGRAL MEDICAL PRODUCTS CO. LTD.·Product code EZD·January 13, 2015

    OUTBACK

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code PDU·July 17, 2014

    UNKNOWN SCREW

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·November 7, 2023

    EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·December 18, 2017

    UNKNOWN SCREW

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·November 7, 2023

    UNKNOWN SCREW

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·November 7, 2023

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code MUM·July 2, 2018

    EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MQR·May 2, 2018

    G7 HI-WALL E1 LINER 32MM C

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code PBI·November 6, 2023

    NeuViz Dual series Computed Tomography (CT) Scanner System, X-Ray System. Part Number: 989605651321. Intended to produce cross-section images of head and body by computer reconstruction of X-ray transmission data taken at different angles.

    FDA Recall
    Terminated ·Neuisys, LLC·Product code JAK·July 21, 2008