BEUDAMED
    9 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021

    FEMORAL HEAD STERILE PRODUCT DO NOT RESTERILIZE 12/14 TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·January 10, 2019

    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·January 10, 2019

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 27, 2013

    DEPUY ASR XL FEM IMP SIZE 45

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·March 2, 2011

    MEDISENSE OPTIUM

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·April 2, 2008

    AVENIR MUELLER, STEM, STANDARD, UNCEMENTED, HA, 3, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·January 10, 2019

    LINER STANDARD 3.5 MM

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·October 21, 2019

    COCR HEADS

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·October 21, 2019