BEUDAMED
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    MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984310·anteriors; shade B2; mould 98

    Skipjack

    FDA UDI
    Seaspine Orthopedics Corporation·10889981139018·Bone Cartridge

    AMRESCO TRIGLYCERIDES REAGENTS (PRODUCTS 7730)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    ANGIOPUMP TUBING SET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EVIS EXERA II BRONCHOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code EOQ·December 17, 2025

    ARCOS MODULAR REVISION SYSTEM STRAIGHT TAPERED SPLINED DISTAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 6, 2018

    DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 28, 2013

    XACT CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIM·February 10, 2011

    EMAX 2 PLUS MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 18, 2013