BEUDAMED
    29 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Ascent POCT System, Centurion POCT System, Spinal Fixation System (SFS), Firebird Spinal Fixation Systems: (Firebird Deformity Spinal Fixation System, Phoenix MIS Spinal Fixation System, Phoenix CDX MIS Spinal Fixation System, JANUS Midline Fixation Screws, Firebird NXG Spinal Fixation System, JANUS Fenestrated Screws), Connector System, FIREBIRD SI Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327466850·LE FORT I PLATE, 10MM ADVANCEMENT, LEFT

    NEO-FIT NEONATAL ENDOTRAC

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL INC.·Product code JAY·April 5, 2021

    NEO-FIT NEONATAL ENDOTRAC

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL INC.·Product code JAY·April 5, 2021

    FULL AUTO TONOMETER MODEL TX-20

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    OXOID PBP2 1 LATEX AGGLUTINATION TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    NEO-FIT NEONATAL ENDOTRAC

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL INC.·Product code JAY·April 5, 2021

    NEO-FIT NEONATAL ENDOTRAC

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL INC.·Product code JAY·April 5, 2021

    PUMP MMT-512NAB PRDGM INSULIN BL EN

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·October 23, 2008

    COULTER LH750 HEMATOLOGY ANALZYER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·August 5, 2011

    PROFEMUR(R) TL STEM

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·July 8, 2013

    CER BIOLOXD MOD HD 28MM -3 NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·May 30, 2019

    G7 OSSEOTI MULTIHOLE 66MM I

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 30, 2019

    ARCOS 19X150MM SPL TPR DIST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 6, 2018

    G7 DUAL MOBILITY LINER 54MM I

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWY·May 30, 2019

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·September 18, 2020

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 28, 2020

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·October 23, 2020

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 28, 2020

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 20, 2021