BEUDAMED
    12 results · 27ms · 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 ×

    SURGICAL SIMPLEX CEMENT

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·May 5, 2010

    SIMPLEX P-JAPANESE TWIN PACK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·March 10, 2010

    SIMPLEX P-JAPANESE TWIN PACK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·August 16, 2010

    POROUS FINN STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·March 5, 2019

    REVEL VENTILATOR

    FDA Adverse Event
    Malfunction ·VYAIRE MEDICAL INC·Product code CBK·September 9, 2024

    M2M ASSY, PKG, REVEL, GRN, DISS, ENGL

    FDA Adverse Event
    Malfunction ·VYAIRE MEDICAL·Product code CBK·April 24, 2024

    ASCENT CLSD BOX PS FMRL LG R

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 21, 2018

    ENDOPATH THORACIC ENDOSCOPIC LINEAR CUTTER RELOAD UNIT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY·Product code GAG·April 2, 1999

    TWIST DRILL/2 X 70 MM, STRYKER

    FDA Adverse Event
    Injury ·HOWMEDICA INC.·Product code HTW·September 4, 1997

    ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·ALARIS MEDICAL SYSTEMS·Product code FPA·February 22, 2001

    ASCENT CLSD BOX PS FMRL LG R

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·July 25, 2017

    18X150 ASCENT FML POROUS STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·May 3, 2017