BEUDAMED
    7 results · 25ms · 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.

    FLOTATION THERAPY BED

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    NA

    FDA UDI
    Zimmer, Inc.·00889024132429·

    Royal Flush Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNTHES (USA) 2.4/2.7 MM LOCKING FOOT MODULE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COMP RVRS 25MM BSPLT HA+ADPTR

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·April 24, 2014

    CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·October 3, 2012

    ACCU-CHECK COMPACT PLUS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·February 15, 2008