BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    SOFT TIP EPIDURAL CATHETER KIT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PEEK Corpectomy

    FDA UDI
    Nuvasive, Inc.·00887517623232·PEEK Corp Core, Ø12x33mm

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704293104·

    NON-BR2000 LARGE BONE BLADES

    FDA UDI
    Peter Brasseler Holdings, LLC·00887919095262·KM71-233

    Resona 7/Resona 7CV/Resona 7EXP/Resona 7S/Resona 7OB Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    VACUETTE BLOOD COLLECTION TUBE 3ML K2E K2EDTA

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NA INC.·Product code JKA·November 2, 2020

    ZIMMER AIR DERMATOME II HANDPIECE

    FDA Adverse Event
    Malfunction ·ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS·Product code GFD·February 1, 2013

    SENSIA SR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code NVZ·January 26, 2011

    X-STOP® INTERSPINOUS SPACER

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NQO·July 31, 2014