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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    21.3 INCH MONOCHROME DIGITAL MAMMOGRAPHY LCD MONITOR MS55I2 (ML21055, MD211G5)

    FDA 510(k)
    FDA Class 2 ·Radiology

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450189603·

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JGS·May 7, 2009

    HYDROFIX VASO SHIELD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWDER FREE VINYL PATIENT EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·June 14, 2016

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·July 1, 2022

    DPE MODULAR W/ID AND ISE600

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·April 13, 2007

    MODULAR ANALYTICS CORE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JGS·March 15, 2013

    OT VERIO SYNC METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 5, 2015

    INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·March 30, 2020

    COBAS 6000 C501MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEM·November 13, 2008

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 1, 2014

    3DKNEE

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code JWH·May 23, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 16, 2011

    ARCHITECT C4000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·February 9, 2023

    PALMAZ STENT UNKNOWN

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code FGE·January 10, 2011

    UNK - CONSTRUCTS: LCP

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·May 25, 2021

    UNK - CONSTRUCTS: LCP

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·May 25, 2021

    UNK - CONSTRUCTS: TOMOFIX PLATE/SCREWS

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·May 25, 2021