BEUDAMED
    32 results · 22ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377047472·RELINE-O Trial, 12mm H Offset Left L-pop

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694034524·Carrying Case OsteoMed Multiproduct

    Zavation

    FDA UDI
    Zavation LLC·00842166131644·Ti3Z CIF 12mmx14mmx8mm -5 deg

    “Paonan” Orthopedic Manual Surgical Instrument (Non-Sterile)

    FDA UDI
    Paonan Biotech Co.,Ltd.·04719878788137·Nerve Retractor 8mm

    Screwdriver

    FDA UDI
    Treace Medical Concepts, Inc.·00810111226646·4.0MM VPCS SCREWDRIVER, CANNULATED

    IdentiTi

    FDA UDI
    ALPHATEC SPINE, INC.·00190376148762·ALIF INST, ROTATING DISTRACTOR, 5°, 8mm

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869683807·MOSS Reducer Shaft

    THERMOFLEX SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CAREMATIX WELLNESS SYSTEM, MODEL CWS-5000.1-B

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·September 26, 2014

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·June 28, 2006

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code LZG·July 30, 2019

    INSYNC

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code LWP·October 10, 2014

    BAB FLEXIBLE FABRIC BANDAGES

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER INC·Product code KGX·March 24, 2022

    KAPPA 900 DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code DXY·October 9, 2013

    ENTERRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LNQ·December 28, 2015

    MYOCARDIAL LEAD

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 10, 2014

    PROCLEAR COMPATIBLES

    FDA Adverse Event
    Injury ·COOPERVISION, INC.·Product code LPL·January 5, 2006

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 24, 2020