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

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    3M Clarity Ultra Self-Ligating Brackets and Adhesive Coated Appliance System

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526768482·GENUMEDI PSS GREEN IV

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517575944·CoRoent Ant TLIF Ti, 8x10x40mm 4°

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486000424·MCK Patellofemoral Component

    FUKUSHIMA SUCTION TUBE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B0991804040·FUKUSHIMA SUCTION TUBE

    FUKUSHIMA SUCTION TUBE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896000322·FUKUSHIMA SUCTION TUBE

    N/A

    FDA UDI
    Ortho Development Corporation·00822409128921·4-in-1 Cut Guide w/ Anterior Lip Size 4

    Distal Adjustment Guide

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215063757·

    ASCENDX VCF REDUCTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EASYQC - CHEMISTRY WITH ELECTROLYTES; CHEMISTRY; ELECTROLYTES KIT; CHEMISTRY CALIBRATOR, CREA-U CLAIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    POLYPROPYLENE

    FDA Adverse Event
    Malfunction ·CP MEDICAL·Product code GAW·January 8, 2020

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 11, 2025

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·May 4, 2018

    MENICON ASRB (ASMOFILCON A) SILICONE HYDROGEL SOFT CONTACT LENS

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·March 18, 2026

    MENICON ASRB (ASMOFILCONA)

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·February 25, 2025

    MENICON ASRB (ASMOFILCONA)

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·January 14, 2025

    BD CONNECTA PLUS3 WHITE PEGS

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·June 5, 2024

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·July 27, 2011

    PREFYX PPS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code FTL·June 20, 2013

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·October 1, 2008