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

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    MODIFIED RETRIEVER (MODIFIED, LINE EXTENSION), MODELS 90152, 90153

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690127246·AK3 PS Insert Trial Size 6, 10mm

    BD INSULIN SYRINGE WITH THE BD ULTRA-FINE NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·June 1, 2020

    HDL-CHOLESTEROL PLUS 2ND GENERATION

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    PERIFIX SAFETY EPIDURAL NEEDLES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BD INSULIN SYRINGE WITH THE BD ULTRA-FINE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·April 6, 2018

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code ESW·December 16, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code ESW·December 16, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code ESW·December 16, 2019

    EVOLUTION ESOPHAGEAL CONTROLLED-RELEASE STENT-FULLY COVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code ESW·March 25, 2015

    M2A-MAGNUM MOD HD SZ 54MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 1, 2026

    PPF LTZ STEM SZ 07X165MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 1, 2026

    5.0MM DIA TPRD HD PER SCRW 45

    FDA Adverse Event
    Injury ·1219655 DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDIC·Product code JDL·May 6, 2013

    ESSURE

    FDA Adverse Event
    Malfunction ·BAYER PHARMA AG·Product code HHS·September 16, 2014

    ANGIOMAT ILLUMENA

    FDA Adverse Event
    Other ·LIEBEL-FLARSHEIM CO.·Product code DXT·April 19, 2011

    Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large 4) Large Long 5) Mini. Allows for positioning directly on the midline keel of the occiput.

    FDA Enforcement
    Class I ·Terminated·Stryker Spine·August 28, 2013

    EVOLUTION® ESOPHAGEAL CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code ESW·November 30, 2021

    EVOLUTION® ESOPHAGEAL CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code ESW·January 17, 2023

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code ESW·December 16, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code ESW·December 18, 2019