BEUDAMED
    12 results · 24ms · Sources: EU EUDAMED, US FDA

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    Augment Off-Axis Instrument System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    10M - Southwest Gas Corp

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588010434·10M - Southwest Gas Corp

    Mui Scientific

    FDA UDI
    H & A Mui Enterprises Inc·10678467508109·Single Use Esophageal 24 Channel Catheter

    VARELISA PR3 ANCA, MODEL NUMBER 17748/17796

    FDA 510(k)
    FDA Class 2 ·Immunology

    CS2 MULTI-HOLE ACETABULAR SHELL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IMPLANT, ENDOSSEOUS, ROOT-FORM

    FDA Adverse Event
    Injury ·J DENTAL CARE SRL·Product code DZE·August 28, 2025

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PML·February 26, 2026

    PUMP MMT-522NAS PRDGM INS V2.2. SK EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·November 21, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Malfunction ·MPROC, VILLALBA·Product code MHY·August 17, 2011

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·July 18, 2013

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code PML·November 13, 2025

    LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

    FDA Adverse Event
    Malfunction ·REYNOSE MANUFACTURING·Product code FKX·August 19, 2011