BEUDAMED
    14 results · 28ms · Sources: EU EUDAMED, US FDA

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    PULPDENT SODIUM HYPOCHLORITE SOLUTION

    FDA 510(k)
    FDA Unclassified ·Unknown

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295244240·P.F.C. SIGMA TIBIAL INSERT FIXED BEARING STABIL...

    ViewPoint 6

    FDA 510(k)
    FDA Class 2 ·Radiology

    UNISIGHT MAMMOGRAPHY VIEWER, MODEL 4.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·February 15, 2023

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code ITI·February 14, 2013

    VASOVIEW HEMOPRO EVH SYSTEM

    FDA Adverse Event
    Injury ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·January 13, 2011

    ARROW WEDGE PRESSURE CATHETER

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL, INC.(SUBSIDIARY OF TELEFLEX, INC.)·Product code DYG·July 17, 2014

    Depuy P.F.C. E Knee System, stabilized plus tibial insert; polyethylene tibial insert, Sz 4, 17.5 mm; Ref 96-2743.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·July 26, 2024

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EFB·September 17, 2025

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·February 18, 2019

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·February 18, 2019

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·February 18, 2019