BEUDAMED
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    Penumbra System Reperfusion Catheter JET 7

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INFRARED THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VISUALIZE: VASCULAR

    FDA 510(k)
    FDA Class 2 ·Radiology

    LINER 28 MM I.D. FOR USE WITH 44/45/46 MM O.D. SHELLS

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code KWY·January 9, 2024

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 24, 2011

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·June 17, 2013

    QUADRA H FEMORAL STEM SIZE 3 LAT SHORT NECK

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·September 25, 2014

    SUREFORM

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code GDW·July 28, 2020

    BD INTIMA-II Y 24GAX0.75IN PRN/EC SLM

    FDA Adverse Event
    Malfunction ·BD SUZHOU (MDS)·Product code FOZ·January 14, 2025

    Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T)

    FDA Enforcement
    Class II ·Ongoing·Medtronic Inc.·November 29, 2017