BEUDAMED
    14 results · 34ms · Sources: EU EUDAMED, US FDA

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    PHACO NEEDLES 1000-R & 1000-O NEEDLES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111062·INSTRUMENT CASE MEDIUM ALUMINUM

    ESSEX ASPIRATION/IRRIGATION INSTRUMENT WITH POSITIONING GUIDE, MODEL SY-1400

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

    FRESENIUS LIBERTY CYCLER

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

    MULTI SPECT 2 [510(K) K913630]

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SYSTEMS·Product code IYX·April 13, 2001

    TI LOW PROFILE SCREW 6.5X30MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 16, 2018

    TI LOW PROFILE SCREW 6.5X20MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 16, 2018

    M/H 3HOLE RLC SHL NRS 54MM/L24

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 7, 2018

    TPRLC 133 MP TYPE1 PPS HO 11.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 7, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013

    S-ROM LINR MSER 10 DEG 28MM C

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code KWZ·December 9, 2010

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·July 9, 2014

    TI LOW PROFILE SCREW 6.5X20MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

    EPOLY 36MM RLC LNR MROM SZ24

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 7, 2018