BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Additive Orthopaedics Patient Specific 3D Locking Lattice Plates

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SpineWorks Anterior Lumbar Device

    FDA UDI
    INNO Holdings, Inc.·M711A1830110·

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515027084·Adjustable Mastoid Retr, spade lft, fork rt, 6 1/2

    8.3MHZ PENCIL PROBE

    FDA UDI
    PARKS MEDICAL ELECTRONICS, INC.·00816787020991·

    ULTICARE SAFETY INSULIN SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SPARTAN S3 FACET SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    I-STAT 6+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·May 22, 2019

    GE OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 3, 2008

    XPRT SLEEP SURFACE

    FDA Adverse Event
    Injury ·STRYKER MEDICAL-KALAMAZOO·Product code IKZ·June 21, 2013

    THERMACHOICE

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code MNB·July 28, 2011