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

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    Filters Regulation: Us FDA ×

    Foundation Dermal Regeneration Scaffold (DRS) Solo

    FDA 510(k)
    FDA Unclassified ·Unknown

    VOLUSON I/E

    FDA 510(k)
    FDA Class 2 ·Radiology

    ALANTECH GRAFT FIXATION SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD PRE-FILLED NORMAL SALINE SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·October 25, 2021

    EVIA DR-T

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·November 6, 2014

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·September 1, 2011

    PELVICOL ACELLULAR AOLLAGEN MATRIX 4X7M

    FDA Adverse Event
    Injury ·COVIDIEN·Product code FTL·July 11, 2013

    UNSPECIFIED BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·October 15, 2025

    BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE 5MG/4MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·May 23, 2024

    Philips Zenition 70, Model Number: 718133

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024