BEUDAMED
    7,530 results · 26ms · Sources: EU EUDAMED, US FDA

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    Compass International

    FDA UDI
    Compass International·B169KCP200·Kelly Coagulation Probe

    ALLEN

    FDA UDI
    HILL-ROM, INC.·00615521014414·Knee Crutch, Pair

    ALLEN

    FDA UDI
    HILL-ROM, INC.·00615521019693·Simplicity Knee Crutch

    KCP PAK CONVENIENCE PACK

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Ultem Koh Cup

    FDA UDI
    Coopersurgical, Inc.·20888937015717·Ultem Koh Cup Non- Conductive - Vaginal Fornice...

    Ultem Koh Cup

    FDA UDI
    Coopersurgical, Inc.·20888937015700·Ultem Koh Cup Non- Conductive - Vaginal Fornice...

    Ultem Koh Cup

    FDA UDI
    Coopersurgical, Inc.·20888937015724·Ultem Koh Cup Non- Conductive - Vaginal Fornice...

    KCP (KELMAN COMPACT PHACO-EMULSIFIER) PEA

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    KCP PAK #2 CONVENIENCE PACK MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    RUMI II KOH-EFFICIENT - UTERINE MANIPULATOR

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HEW·September 21, 2017

    ARTIS ZEEGO

    FDA Adverse Event
    Injury ·SIEMENS HEALTHCARE GMBH·Product code OWB·June 5, 2018

    BD MICROLANCE ¿ 3 NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·January 7, 2022

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, INC.·Product code DRM·March 9, 2007

    EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·January 27, 2021

    The Ultem Polymeric Resin Koh Cup is a non- sterile, reusable vaginal fornices delineator. It is made of medical grade plastics and not made with natural rubber latex. Model Number(s): KCP-30-2

    FDA Enforcement
    Class II ·Ongoing·CooperSurgical, Inc.·June 2, 2021

    The Ultem Polymeric Resin Koh Cup is a non- sterile, reusable vaginal fornices delineator. It is made of medical grade plastics and not made with natural rubber latex. Model Number(s): KCP-30-2

    FDA Recall
    Open, Classified ·CooperSurgical, Inc.·Product code HEW·April 23, 2021

    KOH-EFFICIENT,RUMI,4.0CM

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HEW·April 29, 2022

    REAL INTELLIGENCE CORI

    FDA Adverse Event
    Malfunction ·BLUE BELT TECHNOLOGIES·Product code OLO·February 23, 2023

    REAL INTELLIGENCE CORI

    FDA Adverse Event
    Malfunction ·BLUE BELT TECHNOLOGIES·Product code OLO·February 23, 2023

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·March 26, 2025