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.
    Filters Regulation: Us FDA ×

    CORDIS VANGUARD STEERABLE GUIDEWIRES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Stainless Steel Tibial Nailing System

    FDA UDI
    ORTHOFIX SRL·18033509851179·REVISION LOCKING SCREW STERILE THREAD D 8 MM L...

    VALLEYLAB LAPAROSCOPIC HANDSWITCH/ELECTRODES

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

    STAT PAL SENSYR SYRINGE ASSEMBLY FOR USE W/STATPAL

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION, WORLD WIDE HEADQUARTERS·Product code MKJ·January 17, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 2014

    Transseptal Needle, Trocar. RPN TSNC-18-71.0, TSNC-19-56.0. GPN G02364, G02365. Product consists of a transseptal needle and obturator.

    FDA Enforcement
    Class II ·Terminated·Cook Inc.·November 24, 2021