BEUDAMED
    30 results · 34ms · 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 ×

    CODMAN LUMBAR CATHETER KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code JXG·September 30, 2014

    PROGRAMMABLE VALVE SYSTEM SPECIAL DEVICE

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC./MEDOS S.A.·Product code JXG·August 14, 2006

    CODMAN LUMBER CATHETER KIT

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code JXG·April 11, 2016

    CODMAN LUMBER CATHETER KIT

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES MANSFIELD·Product code JXG·July 15, 2020

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·May 20, 2014

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·November 6, 2012

    SYNVISC (HYLAN G-F 20) INJECTION

    FDA Adverse Event
    Other ·GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·August 27, 2010

    CODMAN LUMBER CATHETER KIT

    FDA Adverse Event
    Injury ·RAYNHAM·Product code JXG·March 9, 2023

    CODMAN LUMBAR CATHETER KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code JXG·July 28, 2014

    CODMAN LUMBER CATHETER KIT

    FDA Adverse Event
    Malfunction ·RAYNHAM·Product code JXG·July 20, 2022

    CODMAN LUMBAR CATHETER KIT

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF·Product code JXG·June 12, 2014

    CODMAN LUMBER CATHETER KIT

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES MANSFIELD·Product code JXG·October 23, 2020

    CODMAN LUMBER CATHETER KIT

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES MANSFIELD·Product code JXG·August 30, 2022

    CODMAN LUMBAR CATHETER KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·December 30, 2013

    CODMAN LUMBAR CATHETER KIT

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC·Product code JXG·November 3, 2014

    NT821707, DRAINAGE KIT, LUMBAR

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code JXG·October 22, 2024

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017