BEUDAMED
    500 results · 85ms · 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.

    CareFusion 213 LLC

    FDA registration
    CareFusion 213 LLC·2 products·🇺🇸 United States

    SENSICLIP

    FDA Adverse Event
    Malfunction ·CAREFUSION 213 LLC·Product code LWK·November 25, 2016

    N/A

    FDA Adverse Event
    CAREFUSION 213 LLC·Product code LWK·January 28, 2014

    *

    FDA Adverse Event
    CAREFUSION 213 LLC·Product code LWK·January 16, 2014

    N/A

    FDA Adverse Event
    CAREFUSION 213 LLC·Product code LWK·January 28, 2014

    N/A

    FDA Adverse Event
    Malfunction ·CAREFUSION 213 LLC·Product code LWK·February 5, 2014

    *

    FDA Adverse Event
    Malfunction ·CAREFUSION 213 LLC·Product code LWK·May 29, 2013

    CHLORAPREP ONE STEP

    FDA Adverse Event
    Malfunction ·CAREFUSION 213, LLC·Product code KXG·April 18, 2024

    RAZOR, SURGICAL

    FDA Adverse Event
    Malfunction ·CAREFUSION 213 LLC·Product code LWK·December 1, 2016

    CAREFUSION SURGICAL CLIPPER

    FDA Adverse Event
    Malfunction ·CAREFUSION 213, LLC·Product code LWK·October 24, 2016

    *

    FDA Adverse Event
    Malfunction ·CAREFUSION 213 LLC·Product code LWK·November 19, 2013

    Sepp, Compound Benzoin Tincture Packaged and Tincture 3,000 Bulk. Product Usage: Preoperative skin product

    FDA Enforcement
    Class III ·Terminated·CareFusion 213, LLC·April 3, 2013

    CHLORAPREP UNKNOWN

    FDA Adverse Event
    Injury ·CAREFUSION 213, LLC 0113·Product code KXG·May 24, 2021

    CHLORAPREP ONE STEP HI-LITE ORANGE

    FDA Adverse Event
    Malfunction ·CAREFUSION 213, LLC 0113·Product code KXG·May 13, 2021

    CHLORAPREP ONE STEP HI-LITE ORANGE

    FDA Adverse Event
    Malfunction ·CAREFUSION 213, LLC 0113·Product code KXG·May 31, 2021

    CHLORAPREP UNKNOWN

    FDA Adverse Event
    Injury ·CAREFUSION 213, LLC 0113·Product code KXG·April 15, 2021

    CHLORAPREP ONE STEP HI-LITE ORANGE

    FDA Adverse Event
    Malfunction ·CAREFUSION 213, LLC 0113·Product code KXG·June 21, 2021

    CHLORAPREP UNKNOWN

    FDA Adverse Event
    Injury ·CAREFUSION 213, LLC 0113·Product code KXG·April 7, 2021

    CHLORAPREP ONE STEP HI-LITE ORANGE

    FDA Adverse Event
    Malfunction ·CAREFUSION 213, LLC 0113·Product code KXG·April 12, 2021

    UNKNOWN CHLORAPREP

    FDA Adverse Event
    Injury ·CAREFUSION 213, LLC 0113·Product code KXF·June 15, 2021