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

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    PG-800A SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DATASCOPE CA 40 8FR. IABS, MODEL 0684-00-04XX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MECHANICAL CHAIR/TRANSPORT CHAIR

    FDA Adverse Event
    GOODBABY·Product code INM·October 1, 2014

    6000 CMS IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 17, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011

    MOZEC¿ RX PTCA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·MERIL LIFE SCIENCES PRIVATE LIMITED·Product code LOX·September 20, 2022

    MOZEC¿ RX PTCA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·MERIL LIFE SCIENCES PRIVATE LIMITED·Product code LOX·September 20, 2022

    40" (102 CM) APPX 5.3 ML ADMIN SET W/2 CHEMOLOCK¿

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·June 13, 2025

    AMISTEM H CEMENTLESS FEMORAL STEM SIZE 3 STD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·December 4, 2015

    Eversense CGM SENSOR (FG-4200-00-301)-Continuous Glucose Monitor

    FDA Enforcement
    Class II ·Terminated·Senseonics, Inc.·November 6, 2019