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

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    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·TRILURON

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·TRILURON®

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·TRILURON® (sodium hyaluronate)

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·TRILURON®

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·TRILURON®

    SOL-M Syringe

    FDA UDI
    Sol-Millennium Medical, Inc.·00818392018219·SOL-M 10ml Luer Lock Syringe w/o Needle

    SOL-M Syringe

    FDA UDI
    Sol-Millennium Medical, Inc.·00818392018240·SOL-M 20ml Luer Lock Syringe w/o Needle

    HydraLok

    FDA UDI
    Choice Spine, LP·10885862129659·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694004862·111 x 191mm Mesh Plate

    NC TREK™ RX Coronary Dilatation Catheter; NC TREK™ OTW Coronary Dilatation Catheter; TREK™ RX Coronary Dilatation Catheter; TREK™ OTW Coronary Dilatation Catheter; MINI TREK™ RX Coronary Dilatation Catheter; MINI TREK™ OTW Coronary Dilatation Catheter; MINI TREK™ II OTW Coronary Dilatation Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Free-Lock®

    FDA UDI
    Zimmer, Inc.·00889024035386·

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC VASCULAR COMPLETE SE VASCULAR STENT SYSTEM

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·VALIANT THORACIC STENT GRAFT SYSTEM

    VALIANT NAVION

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·May 29, 2019

    SOL-MILLENNIUM

    FDA Adverse Event
    Malfunction ·SOL-MILLENNIUM MEDICAL INC., CHICAGO, IL, USA.·Product code FMF·May 16, 2025

    TREK¿

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code LOX·January 7, 2026

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 15, 2014

    FOUNDATION HIP

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code LZO·June 13, 2013

    MINI TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·July 27, 2011

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·Valiant Thoracic Stent Graft with Captiva Delivery System