BEUDAMED
    14 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    ELIA SCL-70S IMMUNOASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    TANDEMHEART PUMP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OUTOLOGOUS SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TOTALSHIELD ZIPPERED SURGICAL TOGA, LARGE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code FYA·December 15, 2014

    ENDOTAK DSP

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code LWS·October 3, 2014

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 31, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 27, 2011

    CAPIOX RX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DTZ·May 26, 2023

    3.5MM CANNULATED LOCKING CORTICAL SCREW, 50MM

    FDA Adverse Event
    Injury ·ORTHOPEDIATRICS·Product code HWC·September 15, 2017

    CAPIOX RX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·April 20, 2018

    CAPIOX RX OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 31, 2024

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DTZ·January 31, 2024

    CAPIOX®RX

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 9, 2024

    CAPIOX RX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 5, 2018