BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

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    MATRIX CR 2050, PMI 3000

    FDA 510(k)
    FDA Class 2 ·Radiology

    Irby Class B 21 - 36 Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588252896·Irby Class B 21 - 36 Metal

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122796·K-WIRE - SINGLE TROCAR THREADED 2.8mm DIA x 230mm

    SURGITEK(R) LUBRI-FLEX(TM) URETERAL STENT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CORDIS BIPAL 7 BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRIME CARE (R) B900

    FDA Adverse Event
    Malfunction ·PRIMUS MEDICAL LLC·Product code FNL·June 23, 2014

    OLYMPUS THUNDERBEAT 5 MM, 45 CM, PISTOL GRIP

    FDA Adverse Event
    Other ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code GEI·January 11, 2013

    MAXIMO DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·December 14, 2010

    ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020