BEUDAMED
    31 results · 25ms · Sources: EU EUDAMED, US FDA

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    MaxBraid BroadBand Suture and Expressbraid BroadBand Graft Manipulation Suture

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

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017842·K-Wire, Double Ended, Trocar Point, Diameter Si...

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017859·K-Wire, Double Ended, Trocar Point, Diameter 0....

    ABX PENTRA 400: LIPOPROTEINS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PREMIUM PLUS DISPOSABLE PROPHY ANGLE MODEL 3399

    FDA 510(k)
    FDA Class 1 ·Dental

    GORE DRYSEAL FLEX INTRODUCER SHEATH

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DYB·October 19, 2020

    PROTECTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·October 10, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·July 7, 2011

    GORE® DRYSEAL FLEX INTRODUCER SHEATH

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DYB·October 6, 2016

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·April 18, 2019

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·March 2, 2020

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·March 18, 2021

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·April 21, 2021

    2.7MM VA-LCP LATERAL DISTAL FIBULA PLATE/4 HOLES/LEFT

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HRS·October 11, 2018

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·June 21, 2019

    GORE® DRYSEAL FLEX INTRODUCER SHEATH

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DYB·May 30, 2023

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·January 25, 2024

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·January 29, 2019

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 12, 2016