BEUDAMED
    275 results · 28ms · Sources: EU EUDAMED, US FDA

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    PM-3

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668102152·BARRAQUER SABLE BRUSH

    STRYKER MEDICAL

    FDA registration
    STRYKER MEDICAL·27 products·🇺🇸 United States

    SAFESKIN* BLUE ZONE POWDER-FREE VINYL EXAM GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    AUTOSURE HT BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ADVANTAGE SERIES 26 OBS 10/04

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·March 13, 2013

    MODEL 722 STRETCHER

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·September 1, 2009

    MODEL 722 STRETCHER

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·September 1, 2009

    MODEL 722 STRETCHER

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·September 1, 2009

    ADVANTAGE SERIES 29 OBS10/04

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·March 11, 2013

    PATIENT ROOM WALL SAVER RECL

    FDA Adverse Event
    Malfunction ·STRYKER CORP, MEDICAL DIV.·Product code FRK·September 10, 2010

    EYE STRETCHER CHAIR

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FMR·January 9, 2013

    1831750-1999-00004

    FDA Adverse Event
    Malfunction ·Product code FPO·May 5, 1999

    1831750-1997-00016

    FDA Adverse Event
    Other ·Product code FNM·September 24, 1997

    1831750-1997-00006

    FDA Adverse Event
    Death ·Product code HDD·April 17, 1997

    1831750-1998-00014

    FDA Adverse Event
    Injury ·Product code KNC·September 18, 1998

    1831750-1998-00010

    FDA Adverse Event
    Other ·Product code FNJ·August 3, 1998

    1831750-2003-00009

    FDA Adverse Event
    Other ·Product code FPO·April 9, 2003

    1831750-1997-00003

    FDA Adverse Event
    Malfunction ·Product code FPO·March 13, 1997

    1831750-1997-00020

    FDA Adverse Event
    Injury ·Product code FPO·December 30, 1997