医疗器械注册管理办法
Medical Devices Registration Administration Method
总则
Chapter 1 General Provisions
  第一条　为规范医疗器械的注册管理，保证医疗器械的安全、有效，根据《医疗器械监督管理条例》，制定本办法。
Article 1 To regulate medical device registration management and ensure their safety and effectiveness of medical device, we set down the management measure according to Regulations for the Supervision and Administration of Medical Device.
  第二条　在中华人民共和国境内销售、使用的医疗器械均应当按照本办法的规定申请注册，未获准注册的医疗器械，不得销售、使用。
Article 2 All the medical device which would like to sell and use within the territory of the Pe
ople’s Republic of China shall apply for registration complying with this measure. These medical devices which not get China registration approval should be prohibited to sell and use.
  第三条　医疗器械注册，是指依照法定程序，对拟上市销售、使用的医疗器械的安全性、有效性进行系统评价，以决定是否同意其销售、使用的过程。
Article 3 Medical device registration is the process of doing systemic evaluation of plan-market medical device on their safety and effectiveness, then decide if medical device can be allowed to sell and use.
第四条　国家对医疗器械实行分类注册管理。
Article 4 The state shall classify medical devices and administer them based on this classification.
  境内第一类医疗器械由设区的市级（食品）药品监督管理机构审查，批准后发给医疗器械注册证书。
Domestic Class I medical devices shall be inspected, approved and granted with a registration certificate by the food drug regulatory authority of the government of the municipalities consisting of districts.
  境内第二类医疗器械由省、自治区、直辖市（食品）药品监督管理部门审查，批准后发给医疗器械注册证书。
Domestic Class II medical devices shall be inspected, approved and granted with a registration certificate by the food drug regulatory authorities of provinces, autonomous regions and municipalities directly under the central government.
  境内第三类医疗器械由国家食品药品监督管理局审查，批准后发给医疗器械注册证书。
Domestic Class III medical device shall be inspected, approved and granted with registration certificate by State Food Drug Administration.
  医疗器械由国家食品药品监督管理局审查，批准后发给医疗器械注册证书。
Imported medical devices shall be inspected, approved and granted with registration certificate by State Food Drug Administration.
  台湾、香港、澳门地区医疗器械的注册，除本办法另有规定外，参照医疗器械办理。
Taiwan, Hongkong and Macao’s medical device registration shall refer to the regulation of imported medical device.
  医疗器械注册证书有效期4年。下载翻译器英文翻中文
Medical devices certificate is valid for 4 years.
  第五条　医疗器械注册证书由国家食品药品监督管理局统一印制，相应内容由审批注册的（食品）药品监督管理部门填写。
Article 5 Medical devices registration certificate shall be pressed by State Food Drug Administration and the content shall be filled in by inspection department of food drug administration.
  注册号的编排方式为：
Registration is arranged as the following:
  ×（×）1(食)药监械（×2）字××××3第×4××5××××6号。其中：
X (X) 1 SFDA (X2) 字××××3第×4××5××××6号
　×1 为注册审批部门所在地的简称：
X  1 :  Shortened form of registration inspection department ‘s locus
  境内第三类医疗器械、医疗器械以及台湾、香港、澳门地区的医疗器械为“国”字；
“国” is for domestic Class III medical devices, imported medical devices and medical devices of Taiwan, Hongkong and Macao.
境内第二类医疗器械为注册审批部门所在的省、自治区、直辖市简称；
  境内第一类医疗器械为注册审批部门所在的省、自治区、直辖市简称加所在设区的市级行
政区域的简称，为××1（无相应设区的市级行政区域时，仅为省、自治区、直辖市的简称）；
  ×2为注册形式（准、进、许）：
  “准”字适用于境内医疗器械；
“进”字适用于医疗器械；
  “许”字适用于台湾、香港、澳门地区的医疗器械；
  ××××3为批准注册年份；
  ×4为产品管理类别；
  ××5为产品品种编码；
  ××××6为注册流水号。
  医疗器械注册证书附有《医疗器械注册登记表》（见本办法附件1），与医疗器械注册证
书同时使用。
Medical device registration certificate is attached with medical device registration record, and shall be used along with medical device registration certificate.
  第六条　生产企业提出医疗器械注册申请，承担相应的法律义务，并在该申请获得批准后持有医疗器械注册证书。
Manufacturers put forward medical device registration application, take relevant regal responsibility and keep medical device registration certificate after getting application approval.
  办理医疗器械注册申请事务的人员应当受生产企业委托，并具有相应的专业知识，熟悉医疗器械注册管理的法律、法规、规章和技术要求。
Individuals who do medical device registration application should be authorized by manufacturer, possess professional knowledge, are familiar with medical device registration administration law, regulation, rules and technical requirement.
  申请医疗器械注册的，生产企业应当在中国境内指定机构作为其代理人，代理人应当承担相应的法律责任；并且，生产企业应当委托中国境内具有相应资格的法人机构或者委托其在华机构承担医疗器械售后服务。
When doing imported medical devices registration, the overseas manufactures shall authorize an unit to be their agent in Chinese territory and the agent should take relevant legal responsibilities.
Meanwhile overseas manufactures shall authorize qualified body corporate or theirs own organ located in China to do after sales service.
  第七条　申请注册的医疗器械，应当有适用的产品标准，可以采用国家标准、行业标准或者制定注册产品标准，但是注册产品标准不得低于国家标准或者行业标准。