BEUDAMED
    23 results · 21ms · Sources: EU EUDAMED, US FDA

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    D 100 L001 PH.I.S.I.O.: NEWBORN HOLLOW FIBER MEMBRANE OXYGENATOR WITH INTEGRATED HARDSHELL CARDIOTOMY/VENOUS RESERVOIR W

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RU NOVOSIBIRSK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·October 16, 2013

    ST JOSEPHS PHOENIX, AZ 1

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code DWF·July 31, 2009

    RU NOVOSIBRIRSK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·April 11, 2013

    RU NOVOSIBIRSK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DWF·October 16, 2013

    CP87170 DE MUENCHEN

    FDA Adverse Event
    Death ·SORIN GROUP ITALIA·Product code DTZ·July 15, 2011

    CP87641 GB SOUTHAMPTON

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DWE·March 22, 2010

    D 100 PH.I.S.I.O. NEWBORN HOLLOW FIBER MEMBRANE OXYGENATOR WITH RESERVOIR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code DTZ·March 28, 2017

    Mini-Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70610311·Mini Sprint-Brackets 5-5 McLaugh/Benn/Trev. .01...

    Kalitec Disc Prep

    FDA UDI
    Kalitec Direct LLC·B07319K0160310·Curette, Forward Angle, #5

    VYSIS UROVYSION BLADDER CANCER RECURRENCE KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    URANUS, COMFORTOUCH LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710610310090·Tri-Channel Met-Traverse, 31mm x 9mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710610310080·Tri-Channel Met-Traverse, 31mm x 8mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710610310100·Tri-Channel Met-Traverse, 31mm x 10mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710610310070·Tri-Channel Met-Traverse, 31mm x 7mm

    ADULT BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE·Product code BTT·May 25, 2007

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·March 26, 2013

    VISIAN ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL·Product code MTA·June 13, 2008

    ENTERPRISE

    FDA Adverse Event
    Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code NJE·April 12, 2011