BEUDAMED
    30 results · 25ms · Sources: EU EUDAMED, US FDA

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    DePuy Synthes Craniomaxillofacial Neuro Devices - MR Conditional

    FDA 510(k)
    FDA Class 2 ·Neurology

    Syringe, Calibration, 3 Liter, Aluminum, Plain Blue, No Logo

    FDA UDI
    A-M SYSTEMS, LLC·00817081026474·Syringe, Calibration, 3 Liter, Aluminum, Plain ...

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180543863·Cervical Cup Curette, Size 3-0, 10°

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180543856·Cervical Cup Curette, Size 3-0, 0°

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180543887·Cervical Cup Curette, Size 3-0, 80°

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180543870·Cervical Cup Curette, Size 3-0, 45°

    MICRUS MICROCATHETER, MODEL COURIER 270

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IMPERIAL SURGICAL LTD. BLANKEY AND SOLUTION WARNING CABINETS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MINICAP TRANSFER SET

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

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·August 24, 2020

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·October 6, 2020

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·October 7, 2020

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·July 14, 2023

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·October 9, 2020

    M3155 INFO CNTR NETWORK DB REL N. O

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code MHX·October 10, 2014

    COULTER® ACT DIFF 2? ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·June 27, 2013

    2600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 22, 2011

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·March 8, 2021

    NI

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·June 8, 2021

    NI

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·February 18, 2022