BEUDAMED
    12 results · 28ms · 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.

    A FLUOROMETER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377017772·RELINE-C Screw, 3.5x40mm FA

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837190767·

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837189297·

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837173227·

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837173821·

    EBI XFIX ACCESS PELVIC FIXATOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RELIANCE LUMBAR IBF SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    28MM DIA COCR MOD HD -6MM NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 15, 2014

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·October 31, 2012

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 2, 2015

    SMALL SUPERIOR AUGMENT GLENOID PLATE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·February 22, 2024