BEUDAMED
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    COULTER(R) MH010

    FDA 510(k)
    FDA Class 2 ·Hematology

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909113852·REVELATION DIAMOND 868-018UF - 5 PACK

    HARDKYDISK NEOMYCIN, 30 MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    DELL ULTRASHARP U3011 W/QUBYX PERFECTLUM BUNDLE

    FDA 510(k)
    FDA Class 2 ·Radiology

    LEVEL 1 HOTLINE LOW FLOW SYSTEMS

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LGZ·January 23, 2024

    LEVEL 1 HOTLINE LOW FLOW SYSTEMS

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LGZ·January 23, 2024

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·January 11, 2013

    BLAKE DRAIN

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code KOG·November 24, 2010

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 3, 2014

    SEE H10

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

    Veradius Unity with Software Release 2.1- Amobile, diagnostic X-ray imaging and viewing system. . Model Number: 718132

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·December 15, 2021