BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    INNERVISION,INC. LAPAROSCOPIC ELECTRODES

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

    PRO

    FDA UDI
    Stryker GmbH·07613327543315·Pelvis Plate Tray

    SHILLA GROWTH GUIDANCE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIO-CHEM ANALYZER, MODEL 100

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PROCEDURAL STRETCHER

    FDA Adverse Event
    Malfunction ·HILLROM DE MEXICO S DE RL DE CV·Product code FPO·April 22, 2014

    PERIGEE WITH INTEPRO SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTP·January 31, 2013

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·December 17, 2010

    NV GXL LNR, +5LAT, 36MM G2-52/54MM CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·May 15, 2024

    NV GXL LNR, +5LAT, 36MM G2-52/54MM CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·May 16, 2024

    Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

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