Article 16 the applicant category ii and category iii medical device registration, it shall submit the clinical test data.
第十六条申请第二类、第三类医疗器械注册，应当提交临床试验资料。
For those who are just joining the series on devfs, read Part 4 of this series, where I explained how devfs solves device registration headaches at the kernel level.
对于那些正在加入devfs系列的人来说，请阅读本系列的第4部分，在那里面我解释了devfs是如何解决内核级设备注册这一令人头疼的问题。
In a portal model, device login and registration might appear identical from the device's point of view, but other services see the portal, not the individual objects.
在门户模型中，从设备的角度来看设备登录和注册可能相同，但其它服务看到的是门户而不是单个对象。
The registration and initialization tasks are taken care of partially by the core kernel and partially by the device driver.
设备的注册和初始化就做这样的事，部份与内核相关，部份与设备驱动相关。
Zhengzhou Good Space Mechanical device Limited company is a machinery and the profession equipment enterprise, is authorizes the registration by National Correlation Department the enterprise.
郑州佳宇机械设备有限公司是一家机械及行业设备的企业，是经国家相关部门批准注册的企业。
These requirements include establishment registration, medical device listing, quality system, medical device reporting, premarket approval or clearance, labeling and U. s. agent requirements.
这些规定包括工厂的注册，医疗设备清单，质量系统，医疗设备报告，售前批准或者认可，商标及美国代理的要求。
Upon registration (904, figure 9), the device searches the device begins the process of communication by discovering other devices (906).
一旦注册(904，图9)，注册设备通过发现其他设备(906)开始通信处理。
Web site to download the entire station device, this edition is the green version of the grandmother, packet containing registration information available.
网站整站下载器，本版是姥姥绿化版，包内附可用注册信息。
In this paper, an EFOV system base on PC-based ultrasound device is presented. A fast algorithms of imaging registration and compound are discussed in detail.
本文给出一种基于PC平台的扩展视野超声成像系统及图像配准和拼接的快速算法。
Repackaging and relabeling of a device and specification development are defined as manufacturing in 21 CFR Part 807, Establishment Registration and Device Listing for Manufacturers of Devices.
在联邦法规第21篇第820.3（o）节和第807 篇以及《器械制造商的企业注册与器械列表》中，均将器械的再包装和再标识以及技术说明制定行为定义为制造。
Congress authorized FDA to collect an annual establishment registration fee for device establishment registrations submitted to the FDA after September 30th, 2007.
国会授权美国食品和药物管理局收取每年设立登记费为器械设立登记，在2007年9月30日后提交给FDA。
Congress authorized FDA to collect an annual establishment registration fee for device establishment registrations submitted to the FDA after September 30th, 2007.
国会授权美国食品和药物管理局收取每年设立登记费为器械设立登记，在2007年9月30日后提交给FDA。
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