BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ULTRA DRIVE 9.5MM DISK DRILL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JXE·September 27, 2012

    ULTRA DRIVE 5MM REVERSE CURETT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JXE·September 27, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·April 30, 2013

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 10, 2011

    PFC SIGMA DIS AUG 8MM, SZ4,RGHT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·August 7, 2008

    MODULAR FEMORAL STEM PRESS-FIT PLASMA SPRAYED CEMENTLESS SIZE 12.5

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·July 18, 2023

    LINER STANDARD 3.5 MM OFFSET 36 MM I.D. FOR USE WITH 56 MM O.D. SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·July 18, 2023

    MODULAR NECK B 12/14 NECK TAPER USE WITH +0 HEADS ONLY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·July 18, 2023