BEUDAMED
    26 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Dynamyx Digital Pathology Software

    FDA 510(k)
    FDA Class 2 ·Pathology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526743588·LEVAMED ANKLE SUPPORT SAND I

    GRYPHON ORTHOCORD

    FDA UDI
    Medos International Sàrl·10886705001255·GRYPHON T BR DS Anchor w/ORTHOCORD TCP/PLGA Abs...

    Zavation

    FDA UDI
    Zavation LLC·00842166132474·Ti3Z CIF 13mmx15mmx11mm -8 deg

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167312108110·

    TALOS® HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167322108110·

    BD INSULIN SYRINGE WITH BD ULTRA-FINE NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·March 3, 2021

    LEKSELL GAMMA KNIFE PERFEXION

    FDA 510(k)
    FDA Class 2 ·Radiology

    PERC-D SPINEWAND

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD INSULIN SYRINGE WITH BD ULTRA-FINE NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·January 6, 2020

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHA·August 12, 2011

    INFIX

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code KWP·August 1, 2014

    INCEPTA

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

    CARDINAL HEALTH

    FDA Adverse Event
    Injury ·CARDINAL HEALTH 200, LLC·Product code KNT·May 8, 2026

    VALIANT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·April 17, 2015

    VALIANT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·April 17, 2015

    TALENT TAA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·April 17, 2015

    TALENT TAA

    FDA Adverse Event
    Injury ·MEDRONIC IRELAND·Product code MIH·April 17, 2015

    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

    GRYPHON T BR DS ANCH W/OC

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code MAI·August 22, 2019