BEUDAMED
    8 results · 17ms · 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 ×

    TPRLC 133 FP TYPE1 BM HO 10.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2019

    FEMORAL HEAD STERILE PRODUCT DO NOT RESTERILIZE 12/14 TAPER

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·April 16, 2019

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·September 19, 2014

    CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·May 25, 2011

    FEMORAL STEM 12/14 NECK TAPER EXT. OFFSET SIZE 2 130 MM STEM LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·September 25, 2017

    FEMORAL HEAD STERILE PRODUCT DO NOT RESTERILIZE 12/14 TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·September 25, 2017

    UNKNOWN

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·April 24, 2014

    TI LOW PROFILE SCREW 6.5X20MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·April 24, 2014