BEUDAMED
    6,004 results · 22ms · Sources: EU EUDAMED, US FDA

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    Uriki Test K

    Device
    EU IVDD · Eu Ivd General ·Iki·On the market

    URIKI BOARD

    Device
    EU IVDD · Eu Ivd General ·Iki·On the market

    Uriki

    Device
    EU IVDR · Eu Ivd Class A ·Iki·On the market

    My Uriki

    Device
    EU IVDR · Eu Ivd Class A ·Iki·On the market·32 countries

    ANI Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ANI Sensor V1 PLUS

    Device
    EU MDR · Eu Md Class 1 ·MDoloris Medical Systems SAS·On the market

    MATOIR EN I ARAMIS

    Device
    EU MDR · Eu Md Class 1 ·groupe lépine·On the market·1 country

    Protection de barrière à poser PositPro 90 cm anis

    Device
    EU MDR · Eu Md Class 1 ·IDENTITES 49·On the market

    Uriki Test K

    Basic UDI-DI
    EU IVDD · Eu Ivd General ·Iki·1 device

    URIKI BOARD

    Basic UDI-DI
    EU IVDD · Eu Ivd General ·Iki·1 device

    Uriki

    Basic UDI-DI
    EU IVDR · Eu Ivd Class A ·Iki·1 device

    My Uriki

    Basic UDI-DI
    EU IVDR · Eu Ivd Class A ·Iki·1 device

    ANI-MR

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·MDoloris Medical Systems SAS·1 device

    Masques à usage médical à élastiques Type II Verts Anis - Sachet de 10

    Device
    EU MDR · Eu Md Class 1 ·VBI Sarl·On the market

    Masques à usage médical à élastiques Type II Verts Anis - Boîte de 50

    Device
    EU MDR · Eu Md Class 1 ·VBI Sarl·On the market

    ANI Sensor V2

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·MDoloris Medical Systems SAS·1 device

    ANI Sensor V1

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·MDoloris Medical Systems SAS·1 device

    ANI Sensor V1 PLUS

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·MDoloris Medical Systems SAS·2 devices

    TDHistology/Cytology Classification name: Calculator/data processing module for clinical use (862.2100). Intended use: Laboratory Information System (L.I.S)

    FDA Enforcement
    Class III ·Terminated·Technidata S.A.·July 24, 2013

    ROSA(TM) Robotized Stereotactic Assistant, Version 2.5 ROSA Surgical Device is a computer-controlled electromechanical arm. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed with three-dimensional imaging software, and uses fiducial markers or optical registration. The system is intended for use by neurosurgeons to guide standard neurosurgical instruments. It is indicated for any neurosurgical condition in which the use of stereotactic surgery may be appropriate.

    FDA Enforcement
    Class II ·Terminated·MEDTECH SAS·June 13, 2018