BEUDAMED
    19 results · 70ms · Sources: EU EUDAMED, US FDA

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    TRIOS, TABLE BASE

    FDA UDI
    MIZUHO ORTHOPEDIC SYSTEMS, INC.·00842430103957·

    TRIOS, TABLE BASE, REFURBISHED

    FDA UDI
    MIZUHO ORTHOPEDIC SYSTEMS, INC.·00842430101670·

    TRIOS, TABLE BASE

    FDA Adverse Event
    Malfunction ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·August 29, 2024

    TRIOS, TABLE BASE

    FDA Adverse Event
    Malfunction ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·August 14, 2024

    TRIOS, TABLE BASE

    FDA Adverse Event
    Injury ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·June 12, 2024

    TRIOS, TABLE BASE

    FDA Adverse Event
    Malfunction ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·January 19, 2026

    TRIOS, TABLE BASE

    FDA Adverse Event
    Malfunction ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·February 25, 2021

    TRIOS, TABLE BASE

    FDA Adverse Event
    Malfunction ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·March 3, 2025

    ASSY, SWIVEL ADAPTER

    FDA Adverse Event
    Malfunction ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·February 12, 2025

    TRIOS ACP TABLE BASE

    FDA Adverse Event
    Malfunction ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·July 26, 2017

    Mizuho OSI Trios, Table Base; Voltage: 100-240V ~ 50/60 Hz Amps: 5,0-5.0A; Model 7803 and 7803AP Orthopaedic: Operating room tablebase - an electronically powered mobile operating table is created, designed for temporary (<24 hours) support and positioning of a patient in a prone, supine, or lateral position depending on the specific table top utilized.

    FDA Enforcement
    Class II ·Terminated·Mizuho OSI·February 17, 2016

    Mizuho OSI Trios, Table Base; Voltage: 100-240V ~ 50/60 Hz Amps: 5,0-5.0A; Model 7803 and 7803AP Orthopaedic: Operating room tablebase - an electronically powered mobile operating table is created, designed for temporary (<24 hours) support and positioning of a patient in a prone, supine, or lateral position depending on the specific table top utilized.

    FDA Recall
    Terminated ·Mizuho OSI·Product code GDC·December 14, 2015

    CHEST SUPPORT SECTION ASSY.

    FDA Adverse Event
    Malfunction ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·July 13, 2021

    FLOWTRON EXCEL TRIO PUMP

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH·Product code JOW·October 21, 2011

    CERVICAL TRACTION VECTOR ADJUSTER

    FDA Adverse Event
    Malfunction ·MIZUHO OSI·Product code JEA·April 4, 2023

    TRULIGHT TRIO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FSY·June 3, 2025

    TRIOS CERVICAL MANAGEMENT BASE UNIT

    FDA Adverse Event
    Injury ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code JEA·March 31, 2026

    UNKNOWN MAYFIELD SKULL CLAMP

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HBL·December 9, 2022

    MAYFIELD MODIFIED SKULL CLAMP

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HBL·March 10, 2023