BEUDAMED
    14 results · 20ms · Sources: EU EUDAMED, US FDA

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    EMIT QST CARBAMAZEPINE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209122882·KIT, IFAK RR + BAG EXTENDED (NO ARS NEEDLE, NO PG)

    GENTLE FLOW BREAST PUMP

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    SPEMBLY 140 CRYOSYSTEM PROBES & TIPS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    D901 LILLIPUT OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·October 13, 2021

    LARGE SUTURECUT NEEDLE DRIVERINSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 6, 2014

    ADULT DUAL-HEATED WITH EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZE·December 3, 2012

    GOODKNIGHT 418G

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code BZD·September 8, 2010

    CUSTOM PERFUSION PACK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·October 30, 2012

    LILLIPUT 1 START

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·April 17, 2023

    LILLIPUT 1 OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALY·Product code DTZ·December 27, 2024

    LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·December 6, 2024

    LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·January 17, 2022

    LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·January 25, 2022