BEUDAMED
    11 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    ReddyPort NIV Access Elbow

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Best Medical International

    FDA UDI
    BEST MEDICAL INTERNATIONAL, INC.·00841365103780·

    OSTEOSCAF

    FDA 510(k)
    FDA Class 2 ·Dental

    ALWAYS MENSTRUAL PADS

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    BELIFU

    FDA Adverse Event
    Injury ·HONG QIANGXING (SHEN ZHEN) ELECTRONICS LIMITED·Product code GZJ·February 10, 2020

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 15, 2014

    6000 CMS IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICES GROUP·Product code FRN·May 23, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 22, 2011

    THREE PEG PATELLA 35MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 13, 2023

    RING TRANSJUGULAR INTRAHEPATIC ACCESS SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·November 15, 2019

    Ingenia 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models: 781342 781377

    FDA Enforcement
    Class II ·Completed·Philips North America Llc·September 15, 2021