BEUDAMED
    26 results · 21ms · Sources: EU EUDAMED, US FDA

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    Coronis Uniti

    FDA 510(k)
    FDA Class 2 ·Radiology

    ProLift Trial

    FDA UDI
    Life Spine, Inc.·00190837088378·

    RTVUE MODEL RTVUE 100

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SCB/STERIS OR-LIGHT INTERFACE BOX

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008348·CONTINUOUS INTERMITTENT SUCTION REGULATORS

    ESON 2 NASAL MASK

    FDA Adverse Event
    Injury ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·August 14, 2019

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008362·CONTINUOUS INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008386·CONTINUOUS INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008379·CONTINUOUS INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008355·CONTINUOUS INTERMITTENT SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072008393·CONTINUOUS INTERMITTENT SUCTION REGULATORS

    AMIA AUTOMATED PD CYCLER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·December 15, 2020

    AMIA AUTOMATED PD CYCLER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·January 12, 2023

    XPRT SLEEP SURFACE

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code IKZ·June 7, 2013

    UNICEL DXC 600 SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·June 24, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 10, 2008

    AMIA AUTOMATED PD CYCLER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·February 15, 2024

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·CODMAN AND SHURTLEFF, INC·Product code NJE·April 27, 2016

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·July 14, 2017

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·July 14, 2017