BEUDAMED
    41 results · 26ms · Sources: EU EUDAMED, US FDA

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    Otoplan

    FDA 510(k)
    FDA Class 2 ·Radiology

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114124·CHARLEUS CORTEX EXTR 23GA 16MM PK/10

    VEO® Lateral Interbody Fusion System

    FDA UDI
    Choice Spine, LP·00840996133401·LATERAL,CONVEX EP SCRAPER,SHAFT

    MUST LT 25MM LONG - PEDICLE SCREW Ø6X45 CANN

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·January 19, 2024

    ENCODER, J6, HIP 190-00137

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·September 19, 2018

    OSSTAPLE, MAXILLOFACIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    STEREOTACTIC FRAME BASED SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    J6 ARM FOR HIP WITH QD

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·September 19, 2018

    MUST LT 03.57.035 MUST LT 15MM SHORT - PEDICLE SCREW Ø7X45 CANN

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·November 18, 2022

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·September 18, 2025

    PEDICLE SCREW MUST LT 15MM SHORT - PEDICLE SCREW Ø4.5X30 CANN

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·November 8, 2023

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWQ·July 16, 2025

    MUST LT 03.59.234 MUST LT 25MM LONG - PEDICLE SCREW Ø7X40 CANN

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·February 16, 2022

    MUST LT 15MM SHORT - PEDICLE SCREW Ø8X40 CANN

    FDA Adverse Event
    Death ·MEDACTA INTERNATIONAL SA·Product code NKB·March 29, 2023

    GLP TRACK END

    FDA Adverse Event
    Malfunction ·ABBOTT AUTOMATION SOLUTIONS GMBH·Product code JQP·May 18, 2026

    ANALYTICAL P MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 17, 2008

    SECURA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·August 11, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 2, 2013

    MUST LT MUST LT 25MM LONG - PEDICLE SCREW 6X45 CANN

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·July 7, 2021

    ENCODER, J6, HIP 190-00137

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·December 8, 2017