BEUDAMED
    10 results · 18ms · 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.

    TMO INTEGRATED CIRCUIT SYSTEM

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971659·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172972274·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971642·

    FERRIS BONE MARROW BIOPSY-ASPIR. NEEDLE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ZOLL FULLY AUTOMATIC AED PLUS

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 9, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 31, 2012

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code MDS·August 30, 2010

    KING LAD SILI CONE SINGLE USE, King Systems, 10 devices/case, ETO Sterile Size 5 / Adult Silicone King LAD¿ Patient Size: >70kg Product Usage: Laryngeal airway

    FDA Enforcement
    Class II ·Terminated·King Systems Corp.·November 28, 2012