BEUDAMED
    40 results · 22ms · Sources: EU EUDAMED, US FDA

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    CELLSEARCH CIRCULATING TUMOR CELL KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707000211·PALATAL EXPANSION SCREW S/STEEL 13mm .

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193104416·HA PEEK EVOS Curved, , 13mmx9mmx 26mm , BICONVE...

    Shannon Recta Round shank

    FDA UDI
    Gebr. Brasseler GmbH & Co. KG·14053613287828·

    OMNIPORT

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

    LIFESOURCE MODELS UA-787, UA 787PC, UA-787T

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·December 6, 2024

    DPB1 SSP UNITRAY KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORP·Product code MZI·May 24, 2013

    DPB1 SSP UNITRAY KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORP·Product code MZI·May 24, 2013

    DPB1 SSP UNITRAY KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORP·Product code MZI·May 24, 2013

    DPB1 SSP UNITRAY KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORP·Product code MZI·May 24, 2013

    DPB1 SSP UNITRAY KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORP·Product code MZI·May 24, 2013

    DPB1 SSP UNITRAY KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORP·Product code MZI·May 24, 2013

    DPB1 SSP UNITRAY KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORP·Product code MZI·May 24, 2013

    VIASYS

    FDA Adverse Event
    Malfunction ·CAREFUSION 207, INC·Product code CBK·October 26, 2009

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 6, 2011

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·April 16, 2013

    BD FACSDIVA VERSION 6.0 AND 6.1

    FDA Adverse Event
    Malfunction ·BD BIOSCIENCES·Product code GKZ·June 13, 2008

    VIASYS

    FDA Adverse Event
    Other ·CAREFUSION 207, INC·Product code CBK·October 27, 2009

    VIASYS

    FDA Adverse Event
    Other ·CAREFUSION 207, INC.·Product code CBK·October 27, 2009