BEUDAMED
    13 results · 25ms · Sources: EU EUDAMED, US FDA

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    PROVIDENCE CUP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556811580·GLENOID REAMER HANDLE

    POZZI STANDARD WIRE

    FDA UDI
    AMERICAN TOOTH INDUSTRIES·D77201519908210·POZZI STANDARD WIRE .032

    AUTOSCEPTOR-GRAM-POSITIVE MIC PANEL READING

    FDA 510(k)
    FDA Class 2 ·Microbiology

    CHEX SINGLE USE CURVED INTRALUMINAL CIRCULAR STAPLER, MODEL CS 21, CS 25, CS 28, CS 32, CS 21L, CS 25L, CS 28L, CS 32L

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MENTOR CE MED HGT TE W/SUT TABS 650CC

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·September 5, 2025

    INDIGO 1.0CM LASER FIBER

    FDA Adverse Event
    Death ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GEX·June 22, 2006

    ELITE PLUS SZ 2 FLANGED

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS·Product code KWY·March 6, 2013

    CONCERTO II CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·February 15, 2011

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·August 8, 2014

    MENTOR CE MED HGT TE W/SUT TABS 650CC

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·September 5, 2025

    MENTOR CE MED HGT TE W/SUT TABS 650CC

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·September 5, 2025

    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026