BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    SPIN CHEM REAGENT, DETERMINATION OF AST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SINGLE NEEDLE HEMODIALYSIS (BFC-142)

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

    DELTASCAN 2000 SERIES

    FDA 510(k)
    FDA Class 2 ·Radiology

    CE TALL HGT TE W/SUT TAB 350CC

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·March 14, 2025

    DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·May 5, 2014

    ADAPTA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC SINGAPORE OPERATIONS·Product code NVZ·October 15, 2012

    INSYNC II MARQUIS

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NIK·August 10, 2010

    Promote, Sterile EO, Model #/ Part #: 3207-30/60010740-207, 60010740-407; 3207-36/60010743-207, 60010743-407; 3213-36/50022126-001, 60013879-307, 60013879-407, 60013879-707; CD3211-36/100006984,100012548, 100012550, 100016680, 100031621, 100035618, 100035619, 100042487, 100047194; CD3211-36Q/100004091, 100004093,100019784, 100035620, 100042486, 100047054; CD3215-36/100006995, 100010246, 100010247, 100010249, 100010250, 100012569, 100012570, 100034981, 100046577, 100046802, 60019065; CD3215-36Q/100004059, 100004060, 100004061, 100023304, 100030590, 100033678, 100042492, 100046803, 100046906

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