BEUDAMED
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    DISPOSABLE FILTERED INSUFFLATION TUBING SET

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122949·K-WIRE - SINGLE TROCAR 1.6mm DIA x 200mm

    ACON MULTI-CLIN DRUG SCREEN TEST DEVICE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    CROC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRILOGY 200

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·March 5, 2014

    TRANSSEPTAL NEEDLE, BRK 1, 71CM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, AF DIVISION·Product code DRC·December 10, 2010

    DEXTRUS 4137

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO KG·Product code NVZ·December 21, 2012

    SEE H10

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDG·June 4, 2018