说明:双击或选中下面任意单词,将显示该词的音标、读音、翻译等;选中中文或多个词,将显示翻译。
您的位置:首页 -> 句库 -> 医疗器械注册
1.
Medical Device Registration System Comparison between China and USA
我国医疗器械注册制度与美国510K注册的比较
2.
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。
3.
Biological Evaluation of Medical Devices (Ⅱ) from the Perspective of Registration, Review and Evaluation
从注册审评角度看二类医疗器械生物学评价
4.
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
5.
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。
6.
medical apparatus that puts a liquid into a cavity drop by drop.
一滴滴地把药注入身体的医疗器械。
7.
institute of medical instruments and apparatus
医疗仪器及器械研究所
8.
The stethoscope is a medical instrument.
听诊器是一种医疗器械。
9.
(d) Medical apparatus and instruments and pharmaceutical industries;
4.医疗器械、制药工业;
10.
China Association of Medical Devices Industry(CAMDI)
中国医疗器械行业协会
11.
Beijing Medical Equipment Institute
北京医疗器械研究所
12.
Review on the Scientific Supervise and Management of Medical Device through the Subject Characteristic of the Medical Device
从医疗器械的学科特点看医疗器械的科学监管
13.
Class10 Surgical, medical, dental and veterinary apparatus and instruments, artificial limbs, eyes and teeth; orthopaedic articles; suture materials.
商标注册类别10外科、学、科和兽医用仪器及器械,假肢、眼和假牙;矫形用品;缝合用材料。
14.
The Points in the Internal Quality System Audit of Medical Device Testing Institutions
医疗器械检测机构质量体系内审工作中应注意的问题
15.
and medical tools to use outside hospitals.
还发明了于医院之外使用的医疗器械。
16.
The Research on Logistics Management of Medical Device in One Hospital in Shanghai
上海市某医院医疗器械物流管理研究
17.
An inventory analysis of medical devices in one hospital in Shanghai
上海市某医院医疗器械库存状况分析
18.
Medical devices manufactured shall meet the national standard, or professional standards when there are no relevant national standards available.
生产医疗器械,应当符合医疗器械国家标准;没有国家标准的,应当符合医疗器械行业标准。