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

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    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·CORONARY BALLOON DILATATION CATHETER

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·MICROSS-SL(TM) PTCA DILATATION CATHETER

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·MICROSS-SL(TM) PTCA DILATATION CATHETER

    HydraLok

    FDA UDI
    Choice Spine, LP·10885862129680·

    Kinetic Dynamic Anterior Cervical Plate System

    FDA UDI
    Life Spine, Inc.·00190837004941·

    ARROW

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 25, 2023

    CODMAN 3000

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 28, 2023

    CODMAN 3000

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code LKK·July 20, 2023

    CODMAN

    FDA Adverse Event
    Death ·CODMAN & SHURTLEFF·Product code LKK·July 18, 2023

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 019B, 019C, 019E, 019F, 019J, & 019K

    DEPUY/CMW 2G

    FDA Adverse Event
    Injury ·DEPUY CMW - 9610921·Product code LOD·December 27, 2019

    FORTIFY DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code LWS·January 13, 2014

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·October 13, 2010

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·December 19, 2012

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 019B, 019C, 019E, 019F, 019J, & 019K

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 019B, 019C, 019E, 019F, 019J, & 019K

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 019B, 019C, 019E, 019F, 019J, & 019K

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 809A POTERIOR CHAMBER INTRAOCULAR LENS

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 019B, 019C, 019E, 019F, 019J, & 019K

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 734A POSTERIOR CHAMBER INTRAOCULAR LENSES