BEUDAMED
    121 results · 30ms · Sources: EU EUDAMED, US FDA

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    Stimulator, Bone Growth, Non-Invasive

    FDA Pre-Market Approval
    FDA Class 2 ·ManaFuse

    NuVasive

    FDA UDI
    Nuvasive, Inc.·00195377106063·NTS Dilator, 16mm

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193114361·HA PEEK EVOS Straight, ,16mmx11mmx 26mm , FLAT ...

    Bard Stinger Ablation Catheter: Item Numbers 210001 218501 L210001 210002 218502 L210002 210003 218503 L210003 210004 218504 L210004 210005 218505 L210005 210006 218506 L210006 210007 218507 L210007 210015 218516 L210008 210016 218518 L210009 210017 218519 L210010 210018 218520 L210011 210019 218521 L210012 210020 218523 L210013 210023 218524 L210014 210024 218525 L210015 210025 218526 L210016 210026 218527 L210017 210027 218528 L210018 210028 218529 210029 210030

    FDA Recall
    Terminated ·C. R.Bard, Inc./Electrophysiology Division·January 8, 2003

    EXPLOR

    FDA UDI
    Biomet Orthopedics, LLC·00880304210288·

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036033934·

    Anatomic Abutment H4mm L8mm

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118141426·Anatomic Abutment H4mm L8mm

    Anatomic Abutment H4mm L8mm

    FDA UDI
    T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190010935·

    Healing Cap 2mm

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118142867·Healing Cap 2mm

    Healing Cap 2mm

    FDA UDI
    T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190011451·

    TriplePlay

    FDA UDI
    DYMEDIX DIAGNOSTICS, INC.·00817377020896·FM1 - Embla

    Mariner

    FDA UDI
    Seaspine Orthopedics Corporation·10889981140717·Mariner Tray, 6.0mm Pre-Contoured Rod Caddy

    GLOBAL UNITE

    FDA UDI
    DEPUY (IRELAND)·10603295085331·GLOBAL UNITE STANDARD STEM TRIAL, SIZE 16

    Integra DigiFuse Cannulated Intramedullary Fusion System,Integra Total Foot System,Integra CAPTURE Screw System & Integra Ti6 Internal Fixation System,Subtalar MBA System,MetaSurg Subtalar Implant,NewDeal BOLD Screw,NewDeal HALLU Lock Plate System,NewDeal HALLU Plates,QWIX Positioning Screw,SPIN Snap-Off Screw,NewDeal TIBIAXYS System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN EGIA TRI STAPLE

    FDA Adverse Event
    Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·April 17, 2023

    UNKNOWN ENDO GIA SULU

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GDW·May 24, 2023

    INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·February 4, 2025

    Dressing, Wound And Burn, Interactive

    FDA Pre-Market Approval
    FDA Class 3 ·ORCEL BILAYERED CELLULAR MATRIX

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    FDA Pre-Market Approval
    FDA Class 3 ·THERAPY COOL PATH DUO/ SAFIRE BLU DUO ABLATION CATHETER AND IBI 1500T9-CP V1.6 CARDIAC ABLATION GENERATOR

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 27, 2013