BEUDAMED
    159 results · 22ms · Sources: EU EUDAMED, US FDA

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    Catheter, Percutaneous Transluminal Coronary Angioplasty (Ptca), Cutting/Scoring

    FDA Pre-Market Approval
    FDA Class 3 ·Lacrosse NSE ALPHA Coronary Dilatation Catheter

    Catheter, Percutaneous Transluminal Coronary Angioplasty (Ptca), Cutting/Scoring

    FDA Pre-Market Approval
    FDA Class 3 ·Lacrosse NSE ALPHA Coronary Dilatation Catheter

    PRO ADVANTAGE

    FDA UDI
    NATIONAL DISTRIBUTION & CONTRACTING, INC.·M220P2300233·PRO ADVANTAGE PILLOWCASE 21X30 T/P 100/CS

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707022855·CALIBRA BANDS 2ND MOLAR n.SUL 26

    Orthoquest

    FDA UDI
    Young Innovations, Inc.·00843471159392·N Nat M Loop 019X025 24Mm Lo

    Orthoquest

    FDA UDI
    Young Innovations, Inc.·00843471159408·N Nat M Loop 019X025 26Mm Lo

    Orthoquest

    FDA UDI
    Young Innovations, Inc.·00843471159422·N Nat M Loop 019X025 30Mm Lo

    Spreader 17mm

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215067748·

    Orthoquest

    FDA UDI
    Young Innovations, Inc.·00843471159415·N Nat M Loop 019X025 28Mm Lo

    SQUALE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IMPL TAPERED SCR-V MTX 3.7MM 3.5MM 11.5MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·January 8, 2025

    ENDO GIA ULTRA

    FDA Adverse Event
    Malfunction ·US SURGICAL PUERTO RICO·Product code GDW·July 19, 2024

    ALTIUS SYSTEM

    FDA Adverse Event
    Malfunction ·NEUROS MEDICAL INC.·Product code LGW·April 2, 2025

    ALTIUS SYSTEM

    FDA Adverse Event
    Malfunction ·NEUROS MEDICAL INC.·Product code LGW·June 20, 2025

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

    FDA Pre-Market Approval
    FDA Class 3 ·TACTICATH QUARTZ SET

    Qualitative And Quantitative Hepatitis B Virus Antibody Assays

    FDA Pre-Market Approval
    FDA Class 2 ·VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBC IGM REAGENT PAK/CALIBRATOR

    LEAD MODEL 302

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code MUZ·November 12, 2008

    CAPSURE SP

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 31, 2011

    SUNBEAM

    FDA Adverse Event
    Injury ·JARDEN CONSUMER SOLUTIONS, DBA SUNBEAM PRODUCTS·Product code IRT·July 11, 2013

    UNKNOWN ENDO GIA SULU

    FDA Adverse Event
    Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·February 28, 2023