BEUDAMED
    11 results · 28ms · 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.
    Filters Regulation: Us FDA ×

    FOLEY-TEMP

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    FLOEY CATHETER W TEMP

    FDA Adverse Event
    Injury ·DEGANIA SILICONE LTD·Product code DRF·October 17, 2017

    FOLEY CATHETER W TEMP

    FDA Adverse Event
    Malfunction ·DEGANIA SILICONE LTD.·Product code DRF·August 10, 2017

    FOLEY CATHETER W TEMP

    FDA Adverse Event
    Malfunction ·DEGANIA SILICONE LTD.·Product code DRF·August 10, 2017

    FOLEY CATHETER W TEMP

    FDA Adverse Event
    Malfunction ·DEGANIA SILICONE LTD.·Product code KOD·July 7, 2017

    FOLEY CATHETER W TEMP

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV (USD)·Product code DRF·November 9, 2018

    3D INVIVO BY CSIST

    FDA 510(k)
    FDA Class 2 ·Radiology

    ALADDIN

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    QUICK COUPLING FOR K-WIRES

    FDA Adverse Event
    Malfunction ·SYNTHES OBERDORF·Product code HWE·May 25, 2014

    TRIMA ACCEL

    FDA Adverse Event
    Malfunction ·TERUMO BCT·Product code GKT·November 14, 2012

    SIMILE

    FDA Adverse Event
    Injury ·PENTRON CLINICAL·Product code EBF·September 10, 2010