BEUDAMED
    25 results · 29ms · 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 ×

    CARDIO MONITOR CENTER VISION; MODEL S-CV7-00

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65810033921·Gutta Percha Pts CadmiumFree

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·10304040140564·Gutta Percha Pts CadmiumFree

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040099650·Gutta Percha Pts CadmiumFree

    TruForm

    FDA UDI
    Rmo, Inc.·00885797099846·MN 1ST BI BD KT N/L R/L 134

    MULTI-LINK ULTRA

    FDA UDI
    ABBOTT VASCULAR INC.·08717648035494·MULTI-LINK OTW ULTRA Coronary Stent System 5.00...

    MULTI-LINK ULTRA

    FDA UDI
    ABBOTT VASCULAR INC.·08717648035463·MULTI-LINK OTW ULTRA Coronary Stent System 5.00...

    MULTI-LINK ULTRA

    FDA UDI
    ABBOTT VASCULAR INC.·08717648035487·MULTI-LINK OTW ULTRA Coronary Stent System 5.00...

    MULTI-LINK ULTRA

    FDA UDI
    ABBOTT VASCULAR INC.·08717648035470·MULTI-LINK OTW ULTRA Coronary Stent System 5.00...

    SCANLAN® Needle Holders

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159022766·Puskas™ Jacobson Micro Needle Holder

    RESPONSE 2000 HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GLYCOSAL HBA1C TEST

    FDA 510(k)
    FDA Class 2 ·Hematology

    AZURION

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·April 24, 2025

    REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER Ø36/+3MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·December 13, 2021

    RUBY COIL

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·March 21, 2016

    T25 STARDRIVE SHAFT F/MATRIX

    FDA Adverse Event
    Malfunction ·SYNTHES (USA) MONUMENT·Product code HXX·February 28, 2013

    UNICEL® DXC 600 PRO SYNCHRON® CLINICAL SYSTEMS

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JGS·March 1, 2011

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 10.0CM

    FDA Adverse Event
    Malfunction ·COSTA RICA·Product code LTI·February 20, 2008

    REVERSE SHOULDER SYSTEM 04.01.0127 HUMERAL REVERSE HC LINER Ø42/+6MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·November 28, 2022

    TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·August 5, 2015