Tmall medical hall selling this kind of medical equipment is real? Look at the purchase of more people, I do not know whether the formal, understand the people guide.

You are referring to the labeling production, professional known as OEM production mode. This kind of production is the way that is permitted by the drug regulatory department, that is to say, the production mode of the law.

As you described, the registration information has been found in the website of the Drug Administration, then it proves that the product is a regular product that was once allowed to be marketed and sold, but if it has already exceeded the expiration date, the certificate is no longer valid, and at most, it can only prove that it was once a regular product that was allowed to be marketed.

According to medical device registration regulations, medical device product registration is divided into three categories: first registration, re-registration and change of registration. For products that are about to expire, companies should start applying for re-registration half a year before the expiration of the registration certificate.

Metronic Consulting--Professional Medical Device Registration Agency, IVD Registration Agency, Clinical Trial CRO