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 ×

    DISSECTRON PORTABLE UNIT

    FDA 510(k)
    FDA Unclassified ·Unknown

    FiberTak DX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACCESS IMMUNOASSAY SYSTEMS BR MONITOR, AND CALIBRATORS, MODEL(S) 387620,AND 387647

    FDA 510(k)
    FDA Class 2 ·Immunology

    ASSY, PROBE, BLADDERSCAN BVI 9400/9600

    FDA Adverse Event
    Malfunction ·VERATHON MEDICAL·Product code IYO·February 15, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·January 13, 2011

    QUICKSET 1PC FLEX DRILL BIT 35

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·August 1, 2014

    Breast Pack, part number AMS3238(A Breast Pack, part number AMS4419(A Breast Pack, part number AMS4419(B Breast Pack, part number AMS5750 Breast Pack, part number AMS5750(A Breast Pack, part number AMS6120 Breast Pack, part number PSS1784(B Breast Pack, part number PSS2272(A

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017