BEUDAMED
    6 results · 24ms · 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 ×

    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

    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