BEUDAMED
    4 results · 26ms · Sources: EU EUDAMED, US FDA

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    874.4250

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code ERL·September 12, 2012

    PENUMBRA MAX PUMP - INDIGO SYSTEM

    FDA Adverse Event
    Malfunction ·PENUMBRA INC., USA·Product code NRY·August 23, 2018

    VOLBELLA WITH LIDOCAINE

    FDA Adverse Event
    Injury ·ALLERGAN (PRINGY)·Product code LMH·June 17, 2019

    Concentric 7F Balloon Guide Catheter (percutaneous catheter per 21 CFR 870.1250), REF 90072, manufactured by Concentric Medical, Inc., Mountain View, CA Product is indicated for use in facilitating the insertion and guidance of an intravascular catheter into a selected blood vessel in the peripheral and neurovascular systems. The balloon provides temporary vascular occlusion during these and other angiographic procedures. Not intended for use to deliver embolic agents or to perform angioplasty.

    FDA Recall
    Terminated ·Concentric Medical Inc·Product code GBS·February 27, 2009