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MILVUE, a simplified joint-stock company (société par actions simplifiée) with a share capital of 3,370.20 euros, headquartered at 35 rue Vaugelas, 75015 Paris, registered with the Paris Trade and Companies Registry under number 841 005 432, represented by Alexandre Parpaleix, in his capacity as President.

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This website is subject to French law. In accordance with current legislation, site users can request access to, modification of, or deletion of their personal data by writing to dpo@milvue.com.

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The Milvue Suite software, developed by Milvue, is a Class IIa medical device within the meaning of Regulation (EU) 2017/745 (MDR) - notified body: BSI, CE 2797. It is intended to assist healthcare professionals in the analysis of radiological images; clinical evaluation and final diagnosis rely solely on the expertise of the healthcare professional.

Regulatory status and product names vary by market (FDA clearances in the United States, Health Canada licence): see the Solutions pages for the per-product, per-region detail.

For information about the use and features of the product, please read the user guide carefully, available on request: IFU Request.

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The Milvue Suite, developed by Milvue, is a class IIa medical device (EU Regulation 2017/745, notified body BSI, CE 2797). TechCare Report, report-drafting assistance software, is not a medical device.
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