医疗器械CE认证MDR范围是有哪些

MDR医疗器械法规的目的是为医疗器械制定了高标准的质量和安全标准，以满足这些产品的一般安全问题为患者和使用者提供高水平的健康保护，确保医疗器械在欧盟单一市场内的自由流通。
MDR不仅包含了MDD及AIMDD涵盖的所有产品；还覆盖专门用于器械的清洁、消毒或灭菌的器械，以及AnnexXVI列举的无预期医疗目的的产品，如美瞳、面部填充或注射、纹身、皮肤改善和美容等产品。
1.包含某些药械结合产品，详细请见Article1（8，9）。
2.包含某些由非活性或处理为非活性的人类来源组织或细胞衍生物制造的特定产品。
3.包含声称仅具有美容目的或另一种非医疗目的，但在功能和风险特征方面类似于医疗器械的特定产品组
4.声明纳米材料器械属于MDR范围，且要接受zui为严格的评估程序。
5.包含发射离子辐射的器械和医疗用途的软件。

The purpose of the MDR medical device regulation is to establisha high standard of quality and safety for medical devices, to meetthe general safety problems of these products, to provide patientsand users with a high level of health protection, and to ensure thefree circulation of medical devices in the EU single market.

MDR not only includes all products covered by MDD and AIMDD; Italso covers the devices specially used for cleaning, disinfectingor sterilizing the devices, as well as the products listed byAnnexXVI that have no intended medical purpose, such as eye beauty,facial filling or injection, tattoo, skin improvement and beautyproducts.

1. It contains some combination products of medicine andmachinery. See Article 1 (8, 9) for details.

2. Contains certain products manufactured from tissue or cellderivatives of human origin that are inactive or treated asinactive.

3. Include specific product groups that claim to have onlycosmetic purpose or another non medical purpose, but are similar tomedical devices in terms of function and risk characteristics

4. Declare that nanomaterial devices belong to the scope of MDRand should be subject to the most rigorous evaluationprocedures.

5. Software containing devices emitting ion radiation andmedical applications.