BEUDAMED
    97 results · 31ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO: RAMP INFLUENZA A/B ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707001300·THREE DIRECT SCREW 2 ANAT INOX 16mm

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690127154·AK3 PS Insert Trial Size 1, 16mm

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471129443·K-WIRE - DOUBLE TROCAR WITH GUIDE 1.1mm DIA x 1...

    DURQ/ QUALIDURA

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CORDIS OPTEASE PERMANENT VENA CAVA FILTER, MODELS 466-F200A, 466-F200B

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BALL HEADS: COCR BALL HEAD 12/14 28 SIZE XL +7

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·November 24, 2020

    STEM: QUADRA-H CEMENTLESS, HA COATED STD STEM SIZE 4

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·February 5, 2021

    VERSAFITCUP DOUBLE MOBILITY HC LINER Ø 58/28

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·July 26, 2016

    MECTACER BIOLOX FORTE CERAMIC BALL HEAD 12/14 Ø 28 SIZE M 0 (USA)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·September 20, 2023

    TRILOGY 200

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code CBK·August 19, 2020

    STEM: AMISTEM H HA COATED LAT STEM SIZE 2

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·June 21, 2019

    QUADRA-H CEMENTLESS, HA COATED STEM SIZE 2 STD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·May 19, 2016

    VERSAFITCUP DM HIGHCROSS ACETABULAR LINER

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code LZO·September 6, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 3, 2013

    ADULT OPEN HEART PACK W/HMO 71000

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP·Product code DTZ·August 21, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN BENNETT CORP.·Product code CBK·April 15, 2011

    CUP: VERSAFITCUP ACETABULAR SHELL Ø 54

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·November 18, 2019

    QUADRA-S 01.12.023 CEMENTLESS, HA COATED STD STEM SIZE 3

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·August 25, 2021

    VERSAFITCUP ACETABULAR SHELL Ø 50

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·June 9, 2016