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

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    ACETABULAR CUP PUSHER/IMPACTOR

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011885305180·dentaform® Band, tooth 36, size 5/Roth 18

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011885305220·dentaform® Band, tooth 36, size 5/Roth 22

    LIFEPORT LOW PROFILE VASCULAR ACCESS PORT W/CATH.

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MODEL UCA / SPEC SYSTEM UCA

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

    TFNA HELICAL BLADE 95MM STERILE

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HSB·September 28, 2016

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 19, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 25, 2010

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·November 21, 2012