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

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    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

    FDA Pre-Market Approval
    FDA Class 3 ·CERAMIC TRANSCEND HIP ARTICULATION

    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

    FDA Pre-Market Approval
    FDA Class 3 ·CERAMIC TRANSCEND ARTICULATION SYSTEM

    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

    FDA Pre-Market Approval
    FDA Class 3 ·CERAMIC TRANSCEND ARTICULATION SYSTEM

    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

    FDA Pre-Market Approval
    FDA Class 3 ·Ceramic Transcend® Hip Articulation System

    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

    FDA Pre-Market Approval
    FDA Class 3 ·CERAMIC TRANSCEND ARTICULATION SYSTEM

    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

    FDA Pre-Market Approval
    FDA Class 3 ·CERAMIC TRANSCEND HIP ARTICULATION

    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

    FDA Pre-Market Approval
    FDA Class 3 ·CERAMIC TRANSCEND ARTICULATION SYSTEM

    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

    FDA Pre-Market Approval
    FDA Class 3 ·CERAMIC TRANSCEND ARTICULATION SYSTEM

    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

    FDA Pre-Market Approval
    FDA Class 3 ·CERAMIC TRANSCEND ARTICULATION SYSTEM

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496030027·WONDER MODEL 70, SIZE XL, GLACE, GRADUATED COMP...

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA UDI
    FX SOLUTIONS·03701037308974·CUTTING GUIDE HOLDER

    MILLENNIUM

    FDA UDI
    Avalign Technologies, Inc.·00190776289256·Bunnell Tendon Stripper,

    NA

    FDA UDI
    STRYKER CORPORATION·34546540756504·1.0MM X 14IN NITINOL GUIDE WIRE

    Stryker

    FDA UDI
    Provision·B504OM2340300270·

    R3 36MM ID US CRMC LINER 54

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·December 2, 2015

    GELFLEX SYNERGY SOFT LENS HIOXFILCON 49% WATER CONTENT CLEAR OR BLUE VISITINT; GELFLEX HIOXIFILCON SOFT CONTACT LENS 49%

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·ANTERIOR CHAMBER INTRAOCULAR LENS (CATARACT)

    Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers

    FDA Pre-Market Approval
    FDA Class 2 ·ELECSYS FREE PSA IMMUNOASSAY/CALSET/CALCHECK

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·August 29, 2023

    TI NUT 11MM WIDTH ACROSS FLATS

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MNH·April 2, 2013