BEUDAMED
    7 results · 18ms · 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 ×

    PAP SMEAR BRUSH

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

    VariTrax Sternal CircumFixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CLO-SURPLUSP.A.D.

    FDA 510(k)
    FDA Unclassified ·Unknown

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·March 25, 2014

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON INC·Product code PAH·November 15, 2012

    CAPSUREEPI

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 10, 2015

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018