BEUDAMED
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    NASOPHARYNGEAL AIRWAY

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    Mediflex Modular III Basic Laparoscopic Instruments

    FDA UDI
    FLEXBAR MACHINE CORPORATION·00842102103773·Modular 3 SA Retention Grasp Ratcheted Handle/S...

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123816·K-WIRE - DOUBLE TROCAR 1.25mm DIA x 125mm

    MINI PATCH

    FDA 510(k)
    FDA Class 2 ·Neurology

    POWDER-FREE-VINYL EXAMINATION GLOVES, COLOR: WHITE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    UMBILICAL CATHETER

    FDA Adverse Event
    Malfunction ·VYGON·Product code FOS·February 17, 2021

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·May 21, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·January 17, 2013

    TOPAZ II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DXY·December 13, 2010

    NAMIC CONVENIENCE KIT SELF REGIONAL HEALTHCARE PV LEG PACK, REF Catalog No. 651919311, UPN Product No. H7496519193111 Product Usage - This needle is intended to be placed over the guidewire to enlarge the opening in the vessel, and is then removed before sliding the catheter over the guidewire

    FDA Enforcement
    Class II ·Terminated·AngioDynamics Inc.·April 13, 2016