BEUDAMED
    6 results · 21ms · 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 ×

    MICROAIRE

    FDA Adverse Event
    Injury ·MICROAIRE SURGICAL INSTRUMENTS·Product code DWH·February 21, 2006

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·January 15, 1998

    CARDIOMEMS¿ HOSPITAL SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code MOM·April 29, 2025

    INOGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·May 8, 2014

    MULTI-LINK VISION CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MAF·October 22, 2012

    PLUM XLM W/DATAPORT

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·August 12, 2010