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

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    2GC HIP/KNEE MODULAR SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    8200 VALVE

    FDA UDI
    HANS RUDOLPH, INC.·00874750008865·8286/8226 LESS 8201 HAND CNTRL

    ASSI

    FDA UDI
    ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORPORATION·00841645119357·Parkes Rasp 17cmCoarse Teeth 8x39mm Flat Under...

    MODIFICATION TO N PROTEIN STANDARD SL

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER

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

    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

    CABLE TENSIONER

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·May 13, 2015

    LIGASURE

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

    M2A-MAGNUM 42-50MM TPR INSRT-3

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 14, 2013

    10MM INZII RETRIEVAL SYSTEM 10/BOX

    FDA Adverse Event
    APPLIED MEDICAL·Product code GCJ·March 22, 2011