BEUDAMED
    56 results · 31ms · 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 Regulation: Us FDA ×

    Plateau Spacer System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L182470120·18mm H x 24mm W x 70mm L XLIF Trial 12 degree L...

    SODIUM HYPOCHLORITE 3 & 6% SOLUTION AND 6% WITH WETTING AGENTS TO LOWER SURFACE TENSION MARKETED AS CHLOR-XTRA

    FDA 510(k)
    FDA Unclassified ·Unknown

    LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER

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

    DARBY

    FDA Adverse Event
    Malfunction ·PRIMA DENTAL GROUP·Product code EJL·November 11, 2024

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 17, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·October 7, 2020

    LIGASURE

    FDA Adverse Event
    Injury ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·July 21, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 20, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 26, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 9, 2021

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 2, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 13, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 16, 2019

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·April 24, 2020

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·March 14, 2019

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 16, 2021

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 28, 2011

    SIMILE

    FDA Adverse Event
    Injury ·PENTRON CLINICAL·Product code EBF·June 21, 2013

    HEARTSTART SLA BATTERY

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code DQA·August 8, 2014