BEUDAMED
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    CRYOSTAB® GENOU PACK

    Device
    EU MDR · Eu Md Class 1 ·GROUPE SOBER SAS·On the market

    CRYOSTAB® GENOU PACK

    Device
    EU MDR · Eu Md Class 1 ·GROUPE SOBER SAS·On the market

    CRYOSTAB® GENOU

    Device
    EU MDR · Eu Md Class 1 ·GROUPE SOBER SAS·On the market

    CRYOSTAB® GENOU

    Device
    EU MDR · Eu Md Class 1 ·GROUPE SOBER SAS·On the market

    CRYOSTAB® GENOU PACK

    Device
    EU MDR · Eu Md Class 1 ·GROUPE SOBER SAS·On the market

    CRYOSTAB® GENOU

    Device
    EU MDR · Eu Md Class 1 ·GROUPE SOBER SAS·On the market

    GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - SOFTWARE ACCESSORIES

    Device
    EU MDD · Eu Md Class 1 ·Synapse medicine·On the market

    EASYMOVE SPATULE T3-T4

    Device
    EU MDR · Eu Md Class 1 ·FOURNITURES HOSPITALIERES INDUSTRIE·On the market·4 countries

    Euro 1400

    Device
    EU MDR · Eu Md Class 1 ·HOME MEDICAL SERVICE H.M.S.·On the market

    URGO K2

    Device
    EU MDR · Eu Md Class 1 ·LABORATOIRES URGO·On the market·1 country

    VARIOUS DIGITAL BIOIMAGING MANAGEMENT INSTRUMENTS - MEDICAL DEVICE SOFTWARE

    Device
    EU MDD · Eu Md Class 2a ·NEHS DIGITAL·On the market·1 country

    Dispositif de compression veineuse élastique de classe 2 de compression

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Laboratoires INNOTHERA·1 device

    CRYOSTAB® GENOU

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·GROUPE SOBER SAS·6 devices

    LABORATOIRE BENEWMEDICAL

    Importer
    🇫🇷 France·4 Manufacturers

    Medicare HTM

    Importer
    🇫🇷 France·5 Manufacturers

    OPHTA-France

    Importer
    🇫🇷 France·8 Manufacturers

    France Chirurgie Instrumentation SAS

    Importer
    🇫🇷 France·13 Manufacturers

    ZYM B Reagent (REF 70493) ZYM B reagent is an additional test used to reveal the results of some miniaturized biochemical test included in the API strips. The API product line is a standardized system combining several biochemical tests, which enables group or species identifications of microorganisms.

    FDA Enforcement
    Class II ·Terminated·Biomerieux France Chemin De L'Or·February 5, 2014

    API NH (REF 10400) API NH is a standardized system for the identification of Neisseria, Haemophilus (and related genera) and Moraxella catharrhalis (Branhamella catarrhalis), which uses miniaturized tests, as well as a specially adapted database. API NH also enables the biotyping of Haemophilus influenza and Haemophilus parainfluenxzae, as well as the detection of a penicllinase.

    FDA Enforcement
    Class II ·Terminated·Biomerieux France Chemin De L'Or·February 5, 2014

    VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated quantitative test for use on the instruments of the VIDAS family for the determination of N terminal fragment of Btype natriuretic peptide in human serum or plasma (lithium heparin) using the ELFA technique (EnzymeLinked Fluorescent Assay). The VIDAS NTproBNP (PBNP) test is used as an aid in the diagnosis of suspected congestive heart failure.

    FDA Enforcement
    Class III ·Terminated·Biomerieux France Chemin De L'Or·September 21, 2016