BEUDAMED
    11 results · 36ms · Sources: EU EUDAMED, US FDA

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    LUXEN 5G

    FDA 510(k)
    FDA Class 2 ·Dental

    LCP

    FDA UDI
    Synthes GmbH·10886982165985·3.5MM LCP T-PLATE 3H HEAD/ 5H SHAFT/67MM-RIGHT ...

    KERBEROS OCCLUDING GUIDE CATHETER AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CT MIDLINE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LUMERA SILTEX HIGH PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·January 31, 2018

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM VG NON US

    FDA Adverse Event
    Injury ·COSTA RICA·Product code LTI·November 19, 2008

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 17, 2011

    SM204 M-SERIES W/BIG WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·July 22, 2013

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·April 14, 2023

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·April 14, 2023

    MultiDiagnost Eleva; x-ray system. Product Codes: 708032, 708036

    FDA Enforcement
    Class II ·Terminated·Philips Electronics North America Corporation·August 10, 2016