Medical device filing certificate is valid for how many years?
Five years.
Medical device filing certificate, the validity of five years, after five years, still want to continue to operate, you can go to the local Food and Drug Administration for renewal, as long as the submission of relevant information can be.
The Medical Device License is valid for five years, and contains the license number, enterprise name, legal representative, person in charge of the enterprise, residence, place of business, mode of operation, scope of business, warehouse address, licensing department, date of issuance and validity period and so on.
Medical device business filing certificate shall contain the number, enterprise name, legal representative, responsible person, residence, place of business, mode of operation, business scope, depot address, filing department, filing date and other matters.
Small program on the sale of medical devices, WeChat can provide "medical device network trading services third-party platform filing certificate"?
WeChat is not the backend of a small program, it's just a medium. There is often more than one third-party platform behind a small program. Currently the medical device online sales management approach has no countermeasure for the filing of small programs.
How to fill in the long-term operation period in the filing form of Class II medical device business?
The filing form inside the time is the filing date to five years later, the business license has is long-term. According to the "supervision and management of medical equipment business approach" Article XV "medical equipment business license" is valid for five years, set out the license number, enterprise name, legal representative, the person in charge of the enterprise, residence, place of business, mode of operation, scope of business, warehouse address, licensing department, date of issuance and validity of the license and other matters.
Medical device business record certificate should contain the number, enterprise name, legal representative, responsible person, residence, place of business, mode of operation, business scope, depot address, filing department, filing date and other matters.
Do I need a warehouse for the filing of Class II medical device vouchers?
Warehouse area of not less than 50 square feet, shall not be set up in the residential
What is the role of the first class of medical equipment filing certificate?
1, the first class of medical devices for the record vouchers include: "Class I medical device for the record voucher" and "Class I medical device production record voucher".
2, "Class I medical device record voucher" is the product of the approval of the certificate, equivalent to the product ID card, with this voucher, the product also has a legitimate registration qualification. 3, "Class I medical device production record voucher" is the product is allowed to produce the approval of the certificate, equivalent to the production license of the enterprise, if there is no such voucher, the enterprise can not produce the product. 4, should be First do the "Class I medical device record voucher", get the voucher to do the "Class I medical device production record voucher". Otherwise, the information of "Class I Medical Device Production Record Voucher" will not be recorded. This is the first to the province in the past to do the first class production registration, and then to the municipal bureau for the first class of the order of registration is just the opposite.