BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    OCULAR FORCE GAUGE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    FIXTEMP C&B

    FDA 510(k)
    FDA Class 2 ·Dental

    NAVITRACK SYSTEM - TOTAL HIP REPLACEMENT CT-FREE

    FDA 510(k)
    FDA Class 2 ·Neurology

    CODA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·October 23, 2017

    UNKNOWN ZIMMER TRILOGY IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDI·May 16, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 17, 2011

    LEAD MODEL 304

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·October 1, 2014

    CODA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·September 10, 2019