1.
The term of validity for the registration certificate of medical devices is four years.
医疗器械产品注册证书有效期四年。
2.
Different and Common Points between Series GB9706.1 Series and GB4793.1 for Medical Apparatus Products;
医疗器械产品标准GB9706.1与GB4793.1的异同
3.
Research on US FDA’s Importing Authorization on Medical Device and Response Measures;
美国FDA对进口医疗器械产品的要求及应对措施
4.
The Comparison Study of American and Chinese Regulatory System of Clinical Laboratory Medical Device;
中美临检类医疗器械产品监管比较研究
5.
Division of Medical Devices Surveillance & Inspection;
构建我国医疗器械产品召回制度的思考
6.
Research on Evaluating Method of Reliability for Medical Apparatus Based on Fuzzy-Evaluating Theory;
医疗器械产品可靠性模糊综合评判方法的研究
7.
Improvement Research on Agent Mode of Medical Equipment of a Company in Guangdong
A公司国外医疗器械产品广东代理模式改进研究
8.
Humanity Consideration on Medical Instruments Product Design
医疗器械产品设计中的人文关怀要素初探
9.
Test Particles of Medical Devices by Coulter Multisizer
用库尔特计数仪检测医疗器械产品中的微粒
10.
Because our products are sterile medical devices for single use, their quality will be adversely affected due to contact between human and products.
因公司生产的产品为一次性无菌医疗器械产品,人员与产品的接触会影响产品的质量.
11.
Medical Instrument Product Quality Illegibility Integration Evaluation Based on the User s Satisfaction;
基于用户满意度的医疗器械产品品质模糊综合评价
12.
Research on Ophthalmic Medical Instrument Reliability Evaluation Method Based on Fuzzy-Gray Theory;
基于模糊灰色理论眼科医疗器械产品质量可靠性评价方法的研究
13.
Precautions of Physical Performance Requirements and Test Methods during Product Standard Drafting Process of Medical Devices
医疗器械产品注册标准起草中物理要求和试验方法应注意的事项
14.
In case a new product has going through the above procedures and is found compliance with requirements, apply to the drug administration department for new product registration.
对完成上述步骤,符合条件的医疗器械产品,向药品监督管理部门申请产品注册。
15.
The Application of Product Lifecycle Management to the Medical Device Industry
医疗器械的产品生命周期管理(PLM)
16.
New Product Development of Our Small & Medium Sized Medical Instruments Enterprises;
我国中小型医疗器械企业的新产品开发
17.
Research and Analysis on Product Quality of the Part of Ⅱ,Ⅲ Category of Medical Device Manufacturers in Hubei Province
对我省部分Ⅱ、Ⅲ类医疗器械生产企业产品质量情况的调研和分析
18.
6-Sigma Technique Application on Medical Device New Product Validation;
六西格玛技术在医疗器械新产品验证项目中的应用