第二、三类医疗器械委托生产备案信息

第二、三类医疗器械委托生产备案信息,包含：企业名称（委托方）、组织机构代码（委托方）、生产许可/备案编号（委托方）、住所（委托方）、生产地址（委托方）、邮编（委托方）、电话（委托方）、法定代表人（委托方）、企业负责人（委托方）、联系人（委托方）、企业名称（受托方）、组织机构代码（受托方）、生产许可/备案编号（受托方）、住所（受托方）、生产地址（受托方）、邮编（受托方）、电话（受托方）、法定代表人（受托方）、企业负责人（受托方）、联系人（受托方）、委托生产产品名称、产品注册号/备案号、委托期限、备案日期、备案部门等信息

Filing Information for Contract Manufacturing of Class II and Class III Medical Devices, including information such as Enterprise Name (Entrusting Party), Organization Code (Entrusting Party), Production License/Filing Number (Entrusting Party), Domicile (Entrusting Party), Production Address (Entrusting Party), Postal Code (Entrusting Party), Telephone Number (Entrusting Party), Legal Representative (Entrusting Party), Enterprise Principal (Entrusting Party), Contact Person (Entrusting Party), Enterprise Name (Entrusted Party), Organization Code (Entrusted Party), Production License/Filing Number (Entrusted Party), Domicile (Entrusted Party), Production Address (Entrusted Party), Postal Code (Entrusted Party), Telephone Number (Entrusted Party), Legal Representative (Entrusted Party), Enterprise Principal (Entrusted Party), Contact Person (Entrusted Party), Name of Contract Manufactured Product, Product Registration Number/Filing Number, Contract Term, Filing Date, Filing Authority, etc.