BEUDAMED
    26 results · 20ms · Sources: EU EUDAMED, US FDA

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    ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Sledgehammer

    FDA UDI
    Keystone Industries·H66810019721·SC 25 lb Pwd Lt Fibered Plus

    GRADIA®

    FDA UDI
    Gc America Inc.·D0470019721·GRADIA® DIRECT Unitips: 20 tips 0.16 mL CV

    GRADIA®

    FDA UDI
    Gc America Inc.·14548161073547·GRADIA® DIRECT Unitips: 20 tips 0.16 mL CV

    SCANLAN® Easy-Tag™ Tracking System

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159033724·Easy-Tag, Pre-Printed, Mini, Green, Loaner, 250/BX

    Bandtite Band Cement

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746061493·BANDTITE GLASS IONOMER POWDER 100 GMS

    Bandtite Band Cement

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746007873·BANDTITE GLASS IONOMER POWDER 100 GMS

    POLYESTER NONABSORBABLE SURGICAL SUTURES URP

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

    SYNTHES (USA) TROCHANTER STABILIZATION PLATE FOR DHS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    QUICK SET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 26, 2025

    DEXTRUS 4137

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·March 13, 2013

    COULTER® LH750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code GKZ·February 27, 2011

    35A AMBULANCE STRETCHER

    FDA Adverse Event
    Injury ·FERNO-WASHINGTON, INC.·Product code FPO·February 21, 2008

    Elements Gutta Percha and Elements RealSeal Cartridges; Part Number: 972-1002, 972-1003, 972-2001, 972-2002

    FDA Recall
    Terminated ·Sybronendo·Product code EKM·October 27, 2009

    2.0MM ASNIS MICRO, CANNULATED SCREWDRIVER, 2.0MM, AO COUPLING

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code LXH·October 20, 2016

    2.0MM ASNIS MICRO, HOLDING SLEEVE FOR 2.0MM SCREWS

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code LXH·January 14, 2016

    APTIMA SARS COV-2

    FDA Adverse Event
    Malfunction ·HOLOGIC, INC.·Product code QJR·February 6, 2023

    2.0MM ASNIS MICRO, CANNULATED SCREWDRIVER, 2.0MM, AO COUPLING

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code LXH·September 18, 2017

    2.0MM ASNIS MICRO, CANNULATED SCREWDRIVER, 2.0MM, AO COUPLING

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code LXH·May 16, 2016

    2.0MM ASNIS MICRO, CANNULATED SCREWDRIVER, 2.0MM, AO COUPLING

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code LXH·May 24, 2016