BEUDAMED
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    EXPD 4343P, EXPD 3643P

    FDA 510(k)
    FDA Class 2 ·Radiology

    SAIPH

    FDA UDI
    MATORTHO LTD·05055455506138·SAIPH Femur Cemented Green Right Size 7

    9.3MHZ PENCIL PROBE 7'

    FDA UDI
    PARKS MEDICAL ELECTRONICS, INC.·00816787021554·

    BWF-5 MEDICAL LASER SERIES

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

    BMR FACE

    FDA 510(k)
    FDA Class 2 ·Neurology

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 22, 2014

    SOLYX SIS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 27, 2013

    HERCULES 3 STAGE BALLOON ESOPHAGEAL

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code KNQ·July 22, 2011

    HANDLE ACETABULAR PRESS

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LXH·May 23, 2025

    ACETABULAR PRESSURIZER SMALL

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LXH·May 23, 2025