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 ×

    SPIROPRO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04047872673167·LEVAMED STABILI-TRI ANK SUP BLU L IV

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694044301·2.3mm x 24mm Mandible Safety Screw

    MODIFIED TO MODULAR FR SEVERE BONE LOSS TRAUMA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACCU-CHEK ACTIVE TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    POLYFORM SYNTHETIC MESH

    FDA Adverse Event
    Injury ·PROXY BIOMEDICAL LTD.·Product code FTL·April 23, 2013

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·April 27, 2011

    PUMP MMT-515LNAS PRDGM INS V2.1 SK EN

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·August 1, 2008