BEUDAMED
    6 results · 26ms · 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 ×

    IMMUNOSUPPRESSANT (WHOLE BLOOD) CONTROL, LEVEL 1 250-1, IMMUNOSUPPRESSANT (WHOLE BLOOS) CONTROL, LEVEL 2, 250-2, IMMUN\S

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    SYNTHES CRANIOFACIAL PLATE AND SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Wireless Pain Relieve Device

    FDA 510(k)
    FDA Class 2 ·Neurology

    NONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code NKB·February 22, 2013

    SWIFT-LOCK ANCHOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·February 2, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·August 5, 2014