BEUDAMED
    8 results · 32ms · 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 ×

    DURASUL, ALPHA INSERT, HOODED, II/32

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·August 3, 2018

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 23, 2011

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 17, 2013

    GE OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·September 19, 2008

    AVENIR MULLER STEM 5 STANDARD

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·January 8, 2026

    ALLOFIT ALLOCLAS SHELL 56/KK

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·January 8, 2026

    DURAL ALPHA INSERT NEUTR KK/32

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·January 8, 2026

    REVITAN®, DISTAL PART, CURVED, UNCEMENTED, 20/140

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KWA·August 9, 2022