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

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    MIDAS TOUCH NITRILE EXAMINATION GLOVES-POWDERFREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Custom Procedure Kit

    FDA UDI
    MEDIVATORS INC.·40677964001770·The ENDO CARRY-ON Procedure Kit contains all of...

    TruFlex™

    FDA UDI
    Ortho Organizers, Inc.·00190707127343·Truflex™ PT SE NiTi Lower 19x25 28mm (10PK)

    TruFlex

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730011893·Truflex™ PT SE NiTi Lower 19x25 28mm 10/PK

    GeneXpert Dx System

    FDA UDI
    CEPHEID·07332940003388·XPERT, GENEXPERT DX SYSTEM

    CURE LP

    FDA UDI
    MEDITECH SPINE, LLC·B167900001380·

    QB1 NMES System

    FDA UDI
    Motive Health, Inc.·00854816006486·QB1 NMES System; 2X-LARGE, REGULAR, LEFT

    CURE LP

    FDA UDI
    MEDITECH SPINE, LLC·B167S1900001380·

    FlowLogic Agile

    FDA UDI
    SONENDO, INC.·00810209420260·FlowLogic Agile Shaping File 30/.04, 25mm

    CARDIOSAVE HYBRID W/ E/F PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·June 28, 2023

    CARDIOSAVE HYBRID W/ E/F PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·October 31, 2023

    INVIGRA MALE LATEX CONDOM GREEN COLORED AND MINT FLAVORED

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    RAPID RHINO-ANTERIOR 90MM, MODEL RR-A 90, RAPID RHINO-POSTERIOR 100MM, MODEL RR-P 100

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    CARDIOSAVE HYBRID W/ E/F PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·August 21, 2024

    CARDIOSAVE HYBRID W/ E/F PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·August 29, 2024

    CARDIOSAVE HYBRID W/ E/F PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·March 7, 2025

    INTELLIVUE MULTI MEASUREMENT SERVER X2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code DSI·February 25, 2025

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·January 30, 2023

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·October 7, 2022

    CARDIOSAVE HYBRID, TYPE G PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·December 27, 2024