BEUDAMED
    9 results · 36ms · 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.

    EVEREST & JENNING SERIES 5000 MODULAR BED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209134472·

    CAMPYLOBACTER BLOOD-FREE SELECTIVE AGAR BASEQ

    FDA 510(k)
    FDA Class 1 ·Microbiology

    WETS & DRIES

    FDA 510(k)

    LOW PROFILE SCREW, TI, 4.5 X 32MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·July 24, 2018

    CHIBA BIOPSY NEEDLE

    FDA Adverse Event
    Injury ·COOK INC.·Product code DWO·May 19, 2014

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 5, 2010

    ENSEAL G2 CURVED JAW

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·December 3, 2012

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021