BEUDAMED
    590 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Klaitec Special

    FDA UDI
    Kalitec Direct LLC·B073DRK0100150·Counter Torque, Low Profile Assembly

    INSTANT-VIEW METHADONE URINE CASSETTE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ACRY ROCK V.

    FDA UDI
    DENTAL MANUFACTURING SPA·08056865001159·

    8.5mm Cannulated Tap

    FDA UDI
    Osteocentric Technologies, Inc.·00810097802223·8.5mm Cannulated Tap

    Ormco

    FDA UDI
    ORMCO CORPORATION·00889989023862·ARCH D-RECT BRAIDED LWR 021X025

    PediPlates

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132133781·PEDIPLATE CASE BOTTOM

    BD PLASTIPAK 50ML CONCENTRIC LUER LOCK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·February 19, 2021

    BARCOMED 2MP2

    FDA 510(k)
    FDA Class 2 ·Radiology

    ELECSYS THYROGLOBULIN CALCHECK

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    POLY-TAPE, 20 X 500MM

    FDA Adverse Event
    Injury ·XIROS·Product code JDR·December 6, 2011

    MEDTRONIC IPG

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·July 17, 2019

    MEDTRONIC IPG

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·July 17, 2019

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

    HOLDING SLEEVE-LONG FOR MATRIX

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·March 18, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·March 2, 2011

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC INSYNC(TM) BIVENTRICAL PACING SYSTEM

    Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·CONSULTA/SYNCRA CRT-PS

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Consulta CRT-P, Percepta Bipolar CRT-P, Percepta Quadripolar CRT-P, Serena Bipolar CRT-P, Serena Quadripolar CRT-P, Sola

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Attain Bipolar OTW Lead and Attain OTW LV Lead

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Consulta CRT-P, Percepta Bipolar CRT-P, Percepta Quadripolar CRT-P, Serena Bipolar CRT-P, Serena Quadripolar CRT-P, Sola