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

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    PHALINX Hammertoe System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Oticon

    FDA UDI
    Oticon A/S·05707131285690·NERA2 PRO, MINIRITE 312 WL CBE

    PD-CTTU-150252

    FDA UDI
    NAKANISHI INC.·04589551354610·

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690122784·Modular Stem 25mm x 125mm

    IRIS Anterior Cervical Plate System

    FDA UDI
    Life Spine, Inc.·00190837060770·Fixed Angle Double Barrel Drill Guide - 0 degre...

    AC-1 ADAPTER CABLE, 8 PIN AND 12 PIN PHILIPS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MASTER-VU A-SCAN, MV4500

    FDA 510(k)
    FDA Class 2 ·Radiology

    RD SET GE - 12

    FDA Adverse Event
    Malfunction ·Product code DQA·August 13, 2021

    RADIFOCUS OPTITORQUE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022

    RINGLOC-X E1 H/W 56/32MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·April 11, 2025

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·May 29, 2013

    EZ-PRO R4 AMBUL COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·June 10, 2011

    INTERSTIM

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·September 3, 2008

    ProScreen 9 Panel Cup w/Adulterants, Item No. PSCUPA-9BO300

    FDA Enforcement
    Class III ·Terminated·Ameditech Inc·December 30, 2015

    OPTITORQUE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Malfunction ·Product code DQO·January 20, 2021