BEUDAMED
    13 results · 51ms · 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 Status: Injury ×

    KING LT AIRWAY

    FDA Adverse Event
    Injury ·KING SYSTEMS CORP.·Product code CAE·December 16, 2009

    KING LT AIRWAY

    FDA Adverse Event
    Injury ·KING SYSTEMS CORP.·Product code CAE·December 16, 2009

    KING LT-D

    FDA Adverse Event
    Injury ·KING SYSTEMS CORP·Product code CAE·June 19, 2009

    ULTRA FLEX ANESTHESIA CIRCUIT

    FDA Adverse Event
    Injury ·KING SYSTEMS CORP.·Product code CAI·August 20, 1997

    HME BOOSTER

    FDA Adverse Event
    Injury ·KING SYSTEMS CORP.·Product code BTT·March 2, 2007

    KING HME BOOSTER

    FDA Adverse Event
    Injury ·KING SYSTEMS CORP·Product code BTT·December 15, 2006

    HME BOOSTER

    FDA Adverse Event
    Injury ·KING SYSTEMS CORP.·Product code BTT·December 21, 2006

    NON CONDUCTIVE ANESTHESIA CIRCUIT

    FDA Adverse Event
    Injury ·KING SYSTEMS CORP.·Product code CAI·December 20, 1995

    KING SYSTEMS UNIVERSAL TRANSPORT COMPONENT

    FDA Adverse Event
    Injury ·KING SYSTEMS CORP.·Product code CAI·March 18, 1997

    *

    FDA Adverse Event
    Injury ·KING SYSTEMS CORP·Product code CAI·October 20, 1999

    UNIVERSAL F BREATHING CIRCUIT

    FDA Adverse Event
    Injury ·KING SYSTEMS CORP.·Product code CAI·September 6, 1995

    UNIVERSAL F2

    FDA Adverse Event
    Injury ·KING SYSTEMS CORP.·Product code CAI·August 13, 1999

    MODIFIED JACKSON-REES CIRCUIT

    FDA Adverse Event
    Injury ·KING SYSTEM CORP.·Product code CAI·January 25, 1996