BEUDAMED
    1,024 results · 26ms · Sources: EU EUDAMED, US FDA

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    Aluna

    FDA UDI
    KNOX MEDICAL DIAGNOSTICS INC.·00860000654005·Aluna Spirometer

    RadiForce®

    FDA UDI
    EIZO CORPORATION·04995047061328·1MP Color LCD Monitor

    RadiForce®

    FDA UDI
    EIZO CORPORATION·04995047046080·1MP Color LCD Monitor

    RadiForce®

    FDA UDI
    EIZO CORPORATION·04995047050926·2MP Multitouch Color LCD Monitor

    RadiForce®

    FDA UDI
    EIZO CORPORATION·04995047059806·2MP Multitouch Color LCD Monitor

    IROX

    FDA Adverse Event
    Other ·SULZER INTERMEDICS INC.·Product code DTB·May 16, 1997

    FIELD GROUP SHOWER CHAIR

    FDA Adverse Event
    Other ·FGI·Product code INM·March 28, 1994

    BIOSENSE WEBSTER CELSIUS DS DIAGNOSTIC ABLATION DEFLECTABLE 8MM TIP CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code OAD·February 7, 2008

    ISOFLEX S, FGI

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2005

    CURRENT DR FGI

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWS·January 31, 2019

    ASSY US FGI Q

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CRMD·Product code NIK·January 13, 2014

    EZ STEER DS BI-DIRECTIONAL NAVIGATIONAL DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATH

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code OAD·March 26, 2009

    BROVIAC CATHETER

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS, INC.·Product code LJS·March 17, 2026

    HICKMAN CATHETER

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS, INC.·Product code LJS·March 17, 2026

    CATH 5F INFINITI TL JL3.5 100C

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code DQO·February 10, 2011

    AIR INJECTION CANNULA

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code FGY·May 20, 2010

    ACCUPORT

    FDA Adverse Event
    Injury ·ZIMMER KNEE CREATIONS, INC.·Product code FGY·November 16, 2017

    TANDEM XL ERCP CANNULA

    FDA Adverse Event
    Injury ·MICROVASIVE ENDOSCOPY, A DIV OF BOSTON SCIENTIFIC CORP.·Product code FGY·May 26, 2000

    ACCUPORT

    FDA Adverse Event
    Malfunction ·ZIMMER KNEE CREATIONS, INC.·Product code FGY·October 20, 2017

    ACCUPORT SIDE TARGETED CANNULA (SELF-DRILLING)

    FDA Adverse Event
    Malfunction ·KNEE CREATIONS LLC·Product code FGY·January 24, 2013