BEUDAMED
    8,744 results · 39ms · Sources: EU EUDAMED, US FDA

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    Essilor Lao Company Limited

    FDA registration
    Essilor Lao Company Limited·1 product·🇱🇦 Lao People's Democratic Republic

    LEADER LAO CO.,LTD

    FDA registration
    LEADER LAO CO.,LTD·2 products·🇱🇦 Lao People's Democratic Republic

    PRIMED Laos Medical Products Manufacturing Sole Co., Ltd.

    FDA registration
    PRIMED Laos Medical Products Manufacturing Sole Co., Ltd.·4 products·🇱🇦 Lao People's Democratic Republic

    PINNACLE3

    FDA Adverse Event
    Malfunction ·ADAC LABORATORIES·Product code IYE·November 10, 2000

    ARTIS PHENO

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE GMBH·Product code OWB·April 4, 2019

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER (ISRAEL) LTD.·Product code DQK·September 19, 2014

    EVOLUT PRO PLUS VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·January 30, 2025

    ARTIS Pheno, Fluoroscopic X-Ray system, Model Number 10849000

    FDA Enforcement
    Class II ·Terminated·Siemens Medical Solutions USA, Inc·August 1, 2018

    ARTIS Pheno, Fluoroscopic X-Ray system, Model Number 10849000

    FDA Recall
    Terminated ·Siemens Medical Solutions USA, Inc·Product code OWB·May 30, 2018

    EVOLUT FX PLUS VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·October 30, 2025

    VALIANT CAPTIVIA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·May 20, 2015

    COROSKOP TOP

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC.·Product code IZI·January 10, 1997

    ARTISTE MV SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code IYE·November 30, 2012

    ARTIS PHENO

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE GMBH·Product code OWB·April 4, 2019

    ARTIS PHENO

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE GMBH·Product code OWB·April 4, 2019

    VASCULAR SOLUTIONS, INC

    FDA Adverse Event
    Injury ·VASCULAR SOLUTIONS, INC.·Product code NIQ·September 9, 2016

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·April 25, 2012

    STENT INSERTION CATHETER, 3.5 STENT

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON INTERVENTIONAL SERVICES·Product code MAF·October 18, 1995

    LC MECHANICS

    FDA Adverse Event
    Malfunction ·GEMS EUROPE·Product code IZI·March 23, 2004

    EVOLUT FX DCS

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NPT·December 16, 2025