BEUDAMED
    9 results · 36ms · 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 FDA Adverse Event ×

    GYNECARE TVT OBTURATOR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code OTN·February 22, 2023

    TERUMO PERFUSION SYSTEM 8000

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code JOR·December 20, 2010

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·July 17, 2014

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 27, 2012

    GYNECARE TVT OBTURATOR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code OTN·January 6, 2023

    GYNECARE TVT OBTURATOR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code OTN·April 5, 2023

    COMP LK SCR 3.5HEX 4.75X30 ST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·June 29, 2022

    COMP LK SCR 3.5HEX 4.75X25 ST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·June 29, 2022

    COMP LK SCR 3.5HEX 4.75X15 ST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·June 29, 2022