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

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    CHAMPION PHYSIOACOUSTICC RECLINER-TRANSPORTER CHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00681490846882·INSTRUMENT 8951414 14 10MM SGL BARL DIST

    Ceramco® iC

    FDA UDI
    Dentsply International Inc.·D00149514140·13 Shades. Contains Ceramco iC Paste Opaques, P...

    EYE CUP, STERILE 1 AND NON STERILE

    FDA 510(k)
    FDA Unclassified ·Unknown

    IQQA Guide

    FDA 510(k)
    FDA Class 2 ·Radiology

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code DTE·February 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·January 6, 2011

    COULTER LH 500 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·July 22, 2014

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 14, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 3, 2024

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·January 24, 2023

    RADIFOCUS ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·September 26, 2018