BEUDAMED
    7 results · 43ms · 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.

    CENTRALERT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BRACCO INJEENERING TRANSFER SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CLEARTOOTH DIGITAL X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·July 31, 2019

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 27, 2014

    STINGRAY

    FDA Adverse Event
    Injury ·R82 A/S·Product code INM·November 13, 2012

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Injury ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·September 9, 2010