BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Spinal Inner Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526550179·GENUMEDI PT KNEE SUP SILVER R EW III

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707011712·CALIBRA 1ST MOL BANDS W/G8025-03 n.UL 13

    MILTEX LAPAROSCOPIC INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ENDOSCOPIC INTRODUCER

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

    CODMAN MICROSENSOR KIT WITH SKULL BOLT (EACH)

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC·Product code GWM·June 3, 2013

    PLUM XLD 110V L.A.

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·September 12, 2014

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·June 23, 2011

    MEDSYTEM III INFUSION PUMP

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·July 27, 2021

    Alcon Custom Ophthalmic Surgical Procedure Packs

    FDA Enforcement
    Class II ·Terminated·Alcon Research, LLC·April 7, 2021