BEUDAMED
    54 results · 26ms · Sources: EU EUDAMED, US FDA

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    Medical Surgical Mask

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526743601·LEVAMED ANKLE SUPPORT SAND III

    GRYPHON ORTHOCORD

    FDA UDI
    Medos International Sàrl·10886705001279·GRYPHON P BR DS Anchor w/ORTHOCORD TCP/PLGA Abs...

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327507195·3-D CHIN PLATE, LONG

    GRYPHON P BR DS ANCHOR W/OC

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·July 11, 2017

    SIMPLICT

    FDA 510(k)
    FDA Class 2 ·Radiology

    HEADWAY 27 MICROCATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GRYPHON P BR DS ANCHOR W/OC

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code MAI·September 3, 2019

    GRYPHON P BR DS ANCHOR W/OC

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SàRL·Product code MAI·September 3, 2019

    GRYPHON P BR DS ANCHOR W/OC

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·November 29, 2018

    GRYPHON P BR DS ANCHOR W/OC

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·October 3, 2018

    GRYPHON P BR DS ANCHOR W/OC

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·July 6, 2020

    M2A 38MM MOD HD -6MM NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·October 29, 2014

    MEDISENSE OPTIUM

    FDA Adverse Event
    Malfunction ·Product code NBW·August 12, 2011

    VITALITY 2

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 8, 2013

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 5, 2025

    Maquet Coronary Perfusion Cannulae with Balloon Tip, with either self-inflating balloon tip or cone distal tips, straight or right angle, available with proximal end fittings for either 1/4 inch connector or male luer fitting, Model numbers 210800, 210801, 210802, 210803, 210804, 210805, 210806, 210807, 210810, 210811, 210812, 210813, 210814, 210815, 210816, 210817, 215800, 215802, 215803, 215804, 215805, 215806, 215807, 215810, 215811, 215812, 215813, 215814, 215815, 215816, and 215817.

    FDA Recall
    Terminated ·Maquet Cardiovascular·Product code DWF·May 19, 2009

    L3C0600 - CURE PRODUCTS

    FDA Adverse Event
    Malfunction ·CONVATEC INC·Product code GBM·July 19, 2022

    GRYPHON P BR DS ANCHOR W/OC

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code MAI·March 14, 2019

    GRYPHON P BR DS ANCHOR W/OC

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code MAI·March 14, 2019