BEUDAMED
    48 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    OPERON

    FDA Adverse Event
    Injury ·BERCHTOLD GMBH & CO. KG·Product code FWY·March 14, 2012

    SKYTRON

    FDA Adverse Event
    Injury ·SKYTRON·Product code FWY·December 3, 2003

    JACKSON TABLE SYSTEM

    FDA Adverse Event
    Injury ·MIZUHO ORTHOPEDIC SYSTEMS, INC.·Product code FWY·May 14, 2008

    RITLENG PROBE

    FDA Adverse Event
    Injury ·FCI OPHTHALMICS·Product code HNL·January 30, 2010

    FCI RITLENG HOOK

    FDA Adverse Event
    Injury ·FCI SAS·Product code HNQ·February 13, 2024

    RITLENG PROBE S1.1460U

    FDA Adverse Event
    Injury ·FCI OPHTHALMICS·Product code HNL·June 1, 2011

    RITLENG PROBE S1-1460U

    FDA Adverse Event
    Injury ·FCI OPHTHALMICS·Product code OKS·March 5, 2012

    LTX 2WY 30CC CATH

    FDA Adverse Event
    Injury ·MENTOR CORP-MINNESOTA DIVISION·Product code KOD·February 23, 2001

    PED 2WY LATEX CATHETER

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code KOD·February 13, 1998

    FCI PROLONG (LEFT EYE)

    FDA Adverse Event
    Injury ·FCI OPHTHALMICS, INC.·Product code LZU·October 11, 2023

    FCI PROLONG (RIGHT EYE)

    FDA Adverse Event
    Injury ·FCI OPHTHALMICS, INC.·Product code LZU·October 11, 2023

    *

    FDA Adverse Event
    Injury ·FCI OPHTHALMICS, INC.·Product code OKS·February 11, 2015

    PEEL-AWY INTRO KIT 10F 14CM

    FDA Adverse Event
    Injury ·DAIG CORP.·Product code DYB·February 16, 2000

    PEEL-AWY INTRO KIT 10F 14CM

    FDA Adverse Event
    Injury ·DAIG CORP.·Product code DYB·February 18, 2000

    DREAMSTATION AUTO CPAP

    FDA Adverse Event
    Injury ·RESPIRONICS INC·Product code BZD·September 26, 2022

    SINGLE USE BILIARY DRAINAGE STENT V

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code FGE·February 2, 2024

    CARPENTIER-EDWARDS PERIMOUNT MAGNA EASE PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·February 25, 2020

    INFINIA II GANTRY

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS F.I. HAIFA·Product code KPS·June 28, 2005

    NM MILLENNIUM MPR COLLIMATOR

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS, F.I. HAIFA·Product code IZX·December 30, 2004

    INFINIA 3/8 HAWKEYE

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS ISRAEL F.I.·Product code KPS·June 23, 2015