What formalities are required for the production of masks can be produced?

The production of masks need the following procedures:

One, to the industrial and commercial administrative organs to apply for the company's business license;

Two, according to the law engraved company seal;

Three, open a bank account;

Four, apply for registration of tax;

Five, apply for the production of masks production license, the production of masks according to the type of masks need to be handled by the Documents are different, if the production of a class of medical devices class masks, you need to first apply for a class of medical device product registration certificate, and then apply for a disposable medical device production filing certificate; if the production of Class II medical device masks, you need to apply for Class II medical device registration certificate, and then apply for a Class II medical device production certificate;

Sixth, and according to the law, such as health permits.

Legal basis: "Medical Device Supervision and Administration Regulations" Article 8

The state to develop medical device industry planning and policy, medical device innovation into the development of key, innovative medical devices to be prioritized review and approval, to support the clinical promotion and use of innovative medical devices, and to promote the high-quality development of medical device industry. The drug supervision and management department of the state council shall cooperate with the relevant departments of the state council, the implementation of the national medical device industry planning and guiding policies.

Article 21 has been registered Class II, Class III medical device products, its design, raw materials, production processes, scope of application, methods of use and other substantial changes that may affect the safety and effectiveness of the medical device, the registrant shall apply to the original registration department for a change in the registration formalities; other changes shall be in accordance with the provisions of the State Council drug supervision and administration department for the record or Report.

Article 22 of the medical device registration certificate is valid for five years. The expiration of the validity of the need to renew the registration, shall be valid for six months before the expiration of the original registration department to apply for renewal of registration.