BEUDAMED
    7 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.
    Filters Regulation: Us FDA ×

    PLEXUFIX BRACHIAL PLEXUS ANESTH. NEEDLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M3848131650·Screw - Ø1.5 mm x 4.5 mm

    USA SERIES LAPAROSCOPES

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

    MINI-MEDIC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ROTALINK? PLUS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - CORK·Product code MCX·May 15, 2014

    SCREW-IN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    ADVANTA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·August 18, 2010