BEUDAMED
    45 results · 38ms · Sources: EU EUDAMED, US FDA

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    Indy OTW Vascular Retriever

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·December 23, 2016

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·March 23, 2017

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MMX·October 24, 2016

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·February 20, 2019

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MMX·October 29, 2018

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·August 3, 2018

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·September 7, 2016

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·April 30, 2018

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·April 14, 2017

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·June 14, 2018

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·April 20, 2017

    SUTURE PLACEMENT DEVICE AND ACCESSORIES, FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES, LSI R SERIES SUTURE PLACEME

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

    OWL RF PROBES

    FDA 510(k)
    FDA Class 2 ·Neurology

    INDIGO SYSTEM ASPIRATION CATHETER 5

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·November 21, 2016

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·February 12, 2019

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·May 29, 2019

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·January 17, 2020

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·December 7, 2018

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·January 29, 2021