BEUDAMED
    202 results · 20ms · Sources: EU EUDAMED, US FDA

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    Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

    FDA Pre-Market Approval
    FDA Class 2 ·S-ROM POLY-DIAL CONSTRAINED LINER

    Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

    FDA Pre-Market Approval
    FDA Class 2 ·S-ROM POLY-DIAL CONSTRAINED ACETABULAR LINER

    Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

    FDA Pre-Market Approval
    FDA Class 2 ·S-ROM POLY-DAIL CONSTRAINED LINER

    Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

    FDA Pre-Market Approval
    FDA Class 2 ·S-ROM POLY-DIAL CONSTRAINED LINER

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295232384·P.F.C. SIGMA FEMORAL CRUCIATE SUBSTITUTING CEME...

    Titan Reverse Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556863640·CANNULATED DRILL FOR 25 MM CENTRAL PEG

    Titan Reverse Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556863633·CANNULATED DRILL FOR 15 MM CENTRAL PEG

    900UDX URINE PATHOLOGY SYSTEM

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Titan™

    FDA UDI
    Ascension Orthopedics, Inc.·10381780244639·Titan™ Reverse Shoulder System The cannulated d...

    Titan™

    FDA UDI
    Ascension Orthopedics, Inc.·10381780244622·Titan™ Reverse Shoulder System The cannulated d...

    Catheter, Percutaneous (Valvuloplasty)

    FDA Pre-Market Approval
    FDA Class 3 ·INOUE BALLOON CATHETER

    Ventricular (Assist) Bypass

    FDA Pre-Market Approval
    FDA Class 3 ·HeartMate 3™ Left Ventricular Assist System

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code ILS·February 13, 2013

    INTELLIVUE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·December 8, 2010

    HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·July 17, 2014

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·January 6, 2020

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·January 8, 2020

    PATIENT CABLE

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·September 8, 2020

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·May 24, 2019

    HEARTMATE GOGEAR SHOWER BAG

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 19, 2019