BEUDAMED
    10,000 results · 59ms · 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 ×

    ACIS PROTI LOR/S 6 MM H

    FDA Adverse Event
    Injury ·TYBER MEDICAL·Product code MAX·October 30, 2024

    EPILOR PLASTIC LOR

    FDA Adverse Event
    Malfunction ·BD·Product code FMF·October 25, 2013

    CORCORDE BUL LOR 11X10X31

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES SPINE·Product code MQP·December 24, 2014

    TI 4.0X055 LOR ROD

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SàRL CH·Product code KWP·July 14, 2025

    TI 4.0X050 LOR ROD

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SàRL CH·Product code KWP·July 14, 2025

    TI 4.0X075 LOR ROD

    FDA Adverse Event
    Death ·MEDOS INTERNATIONAL SàRL CH·Product code NKG·January 14, 2021

    TI 3.5X080 LOR ROD

    FDA Adverse Event
    Death ·MEDOS INTERNATIONAL SàRL CH·Product code NKG·January 14, 2021

    TI 4.0X075 LOR ROD

    FDA Adverse Event
    Death ·MEDOS INTERNATIONAL SàRL CH·Product code NKG·January 14, 2021

    TI 3.5X085 LOR ROD

    FDA Adverse Event
    Death ·MEDOS INTERNATIONAL SàRL CH·Product code NKG·January 14, 2021

    ROCCIA MULTILIF CAGE 9X34MM, 10 LOR.; ROCCIA MULTILIF CAGE 10X34MM, 10 LOR.

    FDA Adverse Event
    Malfunction ·SILONY·Product code MAX·August 12, 2023

    BD EPILOR¿ PLASTIC LOR SYRINGE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code CAZ·May 9, 2022

    LEOPARD IMPLANT 5DEG, LOR, 28X7

    FDA Adverse Event
    Malfunction ·DEPUY RAYNHAM·Product code MQP·May 29, 2012

    PRODISC-L OR PRODISC-C

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MJO·December 23, 2009

    BD EPILOR¿ PLASTIC LOR SYRINGE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code CAZ·August 17, 2022

    LOR SHELL 60 X 72

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·May 13, 2011

    LEOPARD IMPLANT 5DEG, LOR, 28X7

    FDA Adverse Event
    Injury ·DEPUY RAYNHAM·Product code MQP·August 2, 2012

    LOR SHELL 64 X 76

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·January 11, 2019

    CONCORDE INLINE 5 LOR 9X8X25

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SàRL CH·Product code MAX·September 12, 2018

    BENGAL STACK STD LOR 30MM

    FDA Adverse Event
    Injury ·DEPUY SYNTHES SPINE·Product code MQP·May 23, 2017

    BD EPILOR¿ PLASTIC LOR SYRINGE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code CAZ·August 9, 2017