BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    MONITORING KIT AMK-1

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DISCOSCOPES, CERVICAL ENDOSCOPES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EndoCore

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    DIGITALDIAGNOST

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS DMC GMBH·Product code MQB·May 1, 2014

    PENUMBRA ASPIRATION PUMP CANISTER

    FDA Adverse Event
    Malfunction ·PENUMBRA INC.·Product code BTA·March 15, 2010

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 13, 2012

    EV3 Pipeline Flex Embolization Device with Flex Shield Technology

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021