BEUDAMED
    296 results · 28ms · Sources: EU EUDAMED, US FDA

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    N 800 HF

    FDA 510(k)
    FDA Class 1 ·Radiology

    RESORBABLE BONE SCREW

    FDA UDI
    Biomet Orthopedics, LLC·00880304416192·

    Stealth Lingual

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746113871·COSMETIC BRACKET STEALTH LINGUAL MAND CUSPID 03...

    SELOX SR 53

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code LWS·June 14, 2006

    Sensus Healthcare Superficial X-ray Radiation Therapy System with Ultrasonic Imaging Capabilities

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRIAGE TOX DRUG SCREEN CONTROLS

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    HERAEUS MEDICAL PALACOS R+G BONE CEMENT

    FDA Adverse Event
    Injury ·.·Product code JWH·November 1, 2016

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024207134·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024207110·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024207127·

    PALACOS R 1X40 SINGLE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LOD·May 9, 2017

    TI PEDICLE HOOK/DUAL-OPENING SIDE

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code KWP·February 8, 2013

    FIBER ONE

    FDA Adverse Event
    Malfunction ·AMS INNOVATION CENTER-SILICON VALLEY·Product code GEX·December 7, 2010

    CAPTURE-R SELECT

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSS·July 22, 2014

    BD TRUCOUNT¿ ABSOLUTE COUNTING TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 20, 2024

    NEXGEN MIS STEMMED TIBIAL COMPONENT

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·October 4, 2016

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·DROMOS DR/DR-A AND DROMOS SR/SR-B CARDIAC PACING SYSTEMS

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·HOME MONITORING SYSTEM

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·Edora 8 DR-T; Evity 8 DR-T; Enitra 8 DR-T; Enticos 8 DR-T; Evity 6 DR-T; Enitra 6 DR-T; Edora 8 DR; Enitra 6 DR; Edora 8

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·CYLOS FAMILY OF PULSE GENERATORS