BEUDAMED
    751 results · 31ms · 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 ×

    Central Archive module

    FDA UDI
    ORPHEUS MEDICAL LTD·07290017025087·

    Orpheus CAST App

    FDA UDI
    ORPHEUS MEDICAL LTD·07290017025094·A Windows based desktop widget application that...

    Marie Claire

    FDA UDI
    New York Eye·00754317225310·MC-V9461 MAUVE 54/18/148

    Valerie Spencer

    FDA UDI
    New York Eye·00754317214987·VS-9461 MAUVE 54/18/148

    PROFIT

    FDA UDI
    PANTYMED S.A.·07798128675493·MAU Universal Open Wristband

    Kliik:denmark Eyewear

    FDA UDI
    WestGroupe Optical Inc·00676190646559·

    0800,IPS1,08,N,M,AU,VL,SJ,RDL,PV,SF

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828147842·0800,IPS1,08,N,M,AU,VL,SJ,RDL,PV,SF

    Fysh

    FDA UDI
    WestGroupe Optical Inc·00676190687767·Spectacle Frame

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·February 28, 2014

    ATELLICA CH 930 ANALYZER

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·August 3, 2020

    LATITUDE PROGRAMMING SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OSR·September 19, 2023

    DIMENSION EXL 200

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·January 29, 2016

    DIMENSION VISTA 1500

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·August 6, 2021

    ATELLICA CH 930 ANALYZER

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·August 14, 2025

    RV LEAD

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code LWS·August 12, 2023

    BARDIA 30CC SILICONE-COATED LATEX FOLEY CATHETER

    FDA Adverse Event
    Injury ·BARD SDN. BHD. -8040607·Product code EZC·December 7, 2015

    ORTHO VISION ID-MTS

    FDA Adverse Event
    Malfunction ·ORTHO CLINICAL DIAGNOSTICS·Product code KSZ·June 30, 2021

    ORTHO VISION ID-MTS

    FDA Adverse Event
    Malfunction ·ORTHO CLINICAL DIAGNOSTICS·Product code KSZ·July 7, 2021

    ORTHO VISION ID-MTS

    FDA Adverse Event
    Malfunction ·ORTHO CLINICAL DIAGNOSTICS·Product code KSZ·July 7, 2021

    DIMENSION VISTA 1500

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·July 2, 2021