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Medical devices are divided into three categories. I would like to ask how to tell which category a product belongs to from the product registration certificate.
1, apply classification definition

If you can't find the classification in the classification catalog, you can apply for classification definition. Domestic products can apply to the provincial bureau, and overseas products can apply to the national bureau.

2, the same three types of declaration

Can be submitted directly according to the third category of medical devices.

3. Special products

This special product refers to innovative, priority and combination of medicine and machine, and has its corresponding process, which can quickly judge the category.

Extended data:

Medical devices are classified according to the degree of risk. As we said before, there are three categories:

One is low risk,

The second category is moderate risk.

The third category is high risk.

So you may not have a clear understanding, let's just say,

One is band-AIDS, masks, cotton swabs and disposable gloves.

The second category is mostly products that need one-time disinfection, such as LCD visual acuity charts, optometry instruments, hearing AIDS, wheelchairs and so on. After seeing them, everyone can have an outline and know what is going on.

The third category is products implanted in human body, which is just a general statement, in order to make it easier for everyone to understand. I have an impression in my mind that the specific classification is definitely not so simple and rude.