BEUDAMED
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    XPERT MRSA/SA NASAL ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    X-Box

    FDA UDI
    INNO Holdings, Inc.·M71181008220·PEEK, Ta

    ILIZAROV

    FDA UDI
    Smith & Nephew, Inc.·03596010029775·3 HOLE SHORT PLATE - SMALL BONE FIXATOR

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964055751·Endo Carry-On Procedure Kit

    V.A.T.S. SINGLEY TUTTLE LUNG GRASPING FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896003606·V.A.T.S. SINGLEY TUTTLE LUNG GRASPING FORCEPS W...

    V.A.T.S. SINGLEY TUTTLE LUNG GRASPING FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09921008220·V.A.T.S. SINGLEY TUTTLE LUNG GRASPING FORCEPS W...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450048559·

    N/A

    FDA UDI
    Doppkon GmbH & Co. KG·04262494463679·Curette backward angled D 3mm, L 5mm, WL 120mm

    Monoblock Tibial Trial UC Insert

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215043223·

    AGILENTCOMPONENT MONITORING SYSTEM, AGILENT 24/26, AGILENT MULTI-MEASUREMENT SERVER AND COMPACT PORTABLE PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AB CARDIETTE START 200 HV

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·January 15, 2019

    Widex

    FDA UDI
    Widex A/S·05706069727289·Widex EVOKE E-FM (Cappuccino brown S-110 ) RC coil

    Widex

    FDA UDI
    Widex A/S·05706069727685·Widex EVOKE E-FA (Cappuccino brown S-110 ) Tele...

    Widex

    FDA UDI
    Widex A/S·05706069729689·Widex EVOKE E-FP (Cappuccino brown S-110 ) Tele...

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·September 4, 2019

    TRANS-RAY 7FR. 34CC IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 27, 2024

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 8, 2013

    ENTRAK 2500

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code LLZ·May 12, 2011

    INRATIO

    FDA Adverse Event
    Injury ·HEMOSENSE, INC.·Product code JPA·August 6, 2008