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.

    MODEL 1740 PERSONAL POCKET PROGRAMMER

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    MODELS 841,842,843,851,852 & 853 ELEVATING TRACTIO

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    VISIBLE-HERPES TM TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    LCP SUP-CLAVIC-PL 3.5 7HO LE L110 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES ELMIRA·Product code HRS·July 25, 2013

    SAW 20.1X21.4X4.0X0.6MM FOR PIEZOELECTRIC SYSTEM-STER

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code HWE·September 25, 2017

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 10, 2014

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·October 5, 2010

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·December 10, 2012