BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Endotracheal tube; Reinforced Endotracheal tube

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776177829·HEGAR DILATOR SIZE -

    JMS SYSLOC MINI AVF AND APHERESIS NEEDLE SETS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    HM-LAMP II

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

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·January 11, 2023

    ILAB POLARIS MULTI-MODALITY GUIDANCE SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·March 3, 2025

    ILAB? POLARIS MULTI-MODALITY GUIDANCE SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·May 14, 2026

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 14, 2013

    FOUNDATION KNEE

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code JWH·July 5, 2011

    D-FLEX TRIANGULAR RETRACTOR 80MM 5MM

    FDA Adverse Event
    Injury ·CARDINAL CAREFUSION·Product code GCJ·August 20, 2014