How to write a medical device supplier name change application ah

Class II "medical device registration certificate" (change) application form enterprise name product registration certificate No. food and drug supervision and supervision of mechanical (quasi) 200 No. 2 the original approval of the time of the registration certificate changes in the situation of the project originally approved matters applying for a change in matters product name enterprise name registered address production address model, specifications product standards product performance structure and composition of the product scope of application of the product contraindications contact person contact phone number fax e-mail application Changes and reasons for change, based on: Declaration of the unit guarantee this product application unit guarantee: the contents and materials listed in this application form are true and legitimate, the data in the attached information are research and testing of products to visit the data obtained. If there are any inaccuracies, I am willing to assume the corresponding legal responsibility, and bear all the consequences arising therefrom. Signature of the legal representative: January (enterprise seal) review comments Clerk: January Office: January Head of the city, state Food and Drug Administration Bureau of Leadership validation opinion of the Bureau in charge of leadership: January After the change of the registration certificate No. food and drug supervision and regulation of mechanical (quasi) the word 200 No. 2 Remarks: ① two copies of this form, fill in the items that have been changed, no change fill in the "unchanged "; ② before filling out the "Instructions for Filling Out". ▲ Instructions for applicants to fill out: 1, medical device product registration (change) application form. 2, the original registration certificate (submit a copy of the application for change, return the original when you receive). 3, involving the name of the manufacturer, the manufacturer of the change in the registered address and the production of textual changes in the address should also provide the following materials: ① industry and commerce department issued a new business license (or industrial and commercial sector issued the name of the preapproval notification) copy; ② copy of the medical device manufacturer's license. Class Ⅱ Ⅲ are the same