BEUDAMED
    23 results · 31ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    LIFESHIELD LATEX-FREE MICROBORE EXTENSION SET, MODEL 14949 AND OTHERS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EXTENSION SET WITH T-CONN. SL

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·September 21, 2010

    LS LF IV SET CONVRT PP W/BCCK VLV 2CLAVE

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·April 14, 2011

    LS MICROBR EXT SET

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·August 16, 2010

    EXTENSION SET WITH T-CONN. SL

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD.·Product code FPA·March 15, 2012

    EXTENSION SET WITH T-CONN.SL

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·January 21, 2010

    EXTENSION SET WITH T-CONN. SL

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·October 14, 2011

    EXTENSION SET WITH T-CONN.SL

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·January 21, 2010

    LS LF IV SET CONVRT PP W/BCCK VLV 2CLAVE

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·March 14, 2011

    LS MICROBR EXT SET

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD.·Product code FPA·August 17, 2010

    LS LF IV SET CONVRT PP W/BCCK VLV 2CLAVE

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·December 6, 2010

    LS MICROBR EXT SET

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·August 16, 2010

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809845570·FOR MEN 20-30 MM HG KNEE HIGH OPEN TOE LARGE BR...

    NA

    FDA UDI
    Stryker GmbH·00886385005751·Lag Screw, Non-Locking, Self-tap., T6 Drive

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690124597·Modular Offset Stem 17mm x 125mm 2mm

    LYPHOCHEK COAGULATION CONTROL LEVEL 1, LYPHOCHEK COAGULATION LEVEL 2, LYPHOCHEK COAGULATION LEVEL 3, MODELS 781,782,783

    FDA 510(k)
    FDA Class 2 ·Hematology

    DIGITAL BLOOD PRESSURE MONITOR, MODELS HD-503 AND HD-505

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·April 11, 2013

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTL. LTD.·Product code KWA·April 7, 2011

    COBAS INTEGRA 800

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 23, 2008