BEUDAMED
    7 results · 26ms · 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 ×

    MULTI-LUMEN CVC KIT: 3-L 7 FR X 8" (20 C

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code FOZ·October 9, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 5, 2013

    OXFORD UNICOMPARTMENTAL KNEE MENISCAL BEARING

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·July 22, 2011

    FLEXOR URETERAL ACCESS SHEATH AND DILATORS

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FED·January 3, 2020

    FLEXOR URETERAL ACCESS SHEATH AND DILATORS

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FED·January 2, 2020

    FLEXOR URETERAL ACCESS SHEATH AND DILATORS

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FED·January 7, 2020

    IPSOGEN JAK2 PCR KIT IVD

    FDA Adverse Event
    QIAGEN GMBH·Product code PSU·September 4, 2018