BEUDAMED
    13 results · 22ms · Sources: EU EUDAMED, US FDA

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    Virtu C Spinal Implant System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWER CIRCULAR STAPLER DIGITAL LOADING UNIT WITH AND WITHOUT SHEATH

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

    CS 7600

    FDA 510(k)
    FDA Class 2 ·Dental

    PENUMBRA SYSTEM ACE 68 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 14, 2017

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 8, 2017

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·June 11, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 14, 2011

    RSVR MMT-332A 10PK PRDGM 3CC 14L

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code FMF·September 15, 2008

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·October 10, 2017

    2.5 CM BIOPATCH WITH 4.0 MM CENTER HOLE WITH MULTILINGUAL IFU

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES PR·Product code FRO·March 9, 2017

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROVASCULAR·Product code OUT·June 1, 2016

    PENUMBRA SYSTEM REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 4, 2022

    PENUMBRA SYSTEM REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 4, 2022