The control-by-wire mouth gag pertains to medical device field.
这种线控开口器属于医学器械。
The company is developing a proprietary implantable medical device to treat acid reflux.
这家新公司正在开发一项专利，通过向人体植入医疗装置来治疗胃酸倒流。
Now you need to initialize it, and open the socket for the medical device to connect to.
现在您需要对它进行初始化，并打开socket以让医疗设备连接到它。
Implant it in a human body in the form of a medical device, and it will resist the growth of bacteria.
其制成的医疗器件植入人体能抑制细菌繁衍。
While the article below names one particular device, it might also have mentioned a second medical device.
下边的文章命名了特定的一种装置，不过它可能也提及另外第二种医学装置。
It is not a time machine. It's a portable bone-density scanner. A medical device I sell for a living.
并不是时光机器，而是手提骨质密度扫描机，我赖以维生的医疗器材。
The university has collaborated with physicians, funeral directors, citizens and a medical device nonprofit.
这所已经与内科医生，葬礼主管，市民和医用非盈利设备机构建立合作。
CONCLUSIONS Managing every link correctly is the guarantee of the safe use of disposable medical device.
结论抓好每个环节的管理，是一次性使用医疗卫生用品安全使用的保证。
The repository stores the relevant medical device data, lab results, doctor visits, hospitalization records, and so on.
该存储库存储了相关的医疗设备数据、实验室结果、看病历史、住院记录，等等。
More than ever, DSM is helping medical device manufacturers provide better, safer products to improve patient care.
帝斯曼正付出更多努力，帮助医疗器械制造商提供更好、更安全的产品以提升医护质量。
These laboratories may provide services to a number of customers, many of which are not medical device manufacturers.
这些实验室可以向许多客户提供服务，他们中的很多并非医疗器械制造商。
Studies have found that the vast majority of drug and medical device studies are never published in medical journals.
研究表明，绝大部分药品及医疗器械的研究结果都没有在医药杂志上发表过。
The Quality System regulation outlines the minimum elements of a system for designing and producing a medical device.
质量体系法规描述设计和生产医疗器械最少体系要素。
This monthly look at the best-performing biotechnology, drug and medical device stocks is based on data from FactSet Systems.
这个月度的调查着眼于表现最佳的生物科技、制药和医疗设备类股票，以FactSet Systems的数据为基础。
That medical device can be used to determine the gender of a child before birth, prompting some parents to obtain abortions.
B超技术可以观察待产儿的性别，促使一些父母进行流产手术。
This manual incorporates changes required by the Safe Medical Devices Act of 1990 and the Medical Device Amendments of 1992.
本手册合并了1990年医疗器械安全法案及1992年医疗器械修正案的修改要求。
But it found little investor interest in the United States for an early-stage medical device company that had not yet made a profit.
但公司发现，国内没什么投资者对自己这种处于起步阶段还未获得盈利的医疗设备公司感兴趣。
These squirmy larvae are science's newest wonder-cure and were approved in 2003 as the Food &Drug Administration's only live medical device.
这些蠕虫是科学上的奇迹。在2003年，美国食物药品管理局把它门认定为唯一的生物医疗器械。
We're not allowed to turn the phone itself into a medical device, and what that precisely means is currently a grey area in terms of regulation.
不允许我们把手机转为医疗设备，这恰恰意味着目前管理上存在灰色地带。
"We discovered that we had about 400 medical device companies in the state, but these firms didn't see themselves as part of a cluster," he recalls.
他回忆说：“我们发现，全州大约有400家医疗设备企业，但这些企业并不把自己当作集群里的成员。”
The policy takes effect (4) Oct. 1 and also bans accepting gifts from other companies such as medical device makers that do business with the hospitals.
该政策将从10月1日起生效，同时禁止收受象医疗器材制造厂家这样与医院有业务往来的任何公司提供的礼物。
He used the technique recently when programming a prototype of a medical device to help doctors prevent pressure sores in wheelchair-bound patients.
近期在给一种帮助医生预防坐轮椅的病人生褥疮的医疗器械原型机编程时，他就使用了这一方法。
These complaints shall be evaluated to determine whether or not they require reporting to FDA under 21 CFR part 804 or 803, Medical Device reporting.
应对这些投诉进行评估，并根据医疗器械报告制度(联邦法规21篇804或803部)要求决定它们是否需要向FDA报告。
A visit to the hospital or doctor sometime leads to you needing a medical device or equipment, like crutches, a foot brace, a breathing nebulizer, etc.
你去看医生的时候，往往需要购买一些医疗器械或者设备，比如拐杖，足围，气道喷雾器等。
The true value in the RPMS is the ability to discover important patterns or an alarming reading in the medical device message as it flows through the system.
RPMS的真正价值在于能够在医疗设备消息流经系统时从中发现重要的模式或值得引起注意的读数。
That is, the test laboratory is simply a part of a medical device manufacturer of which all device-related divisions shall comply with the QS regulation.
也就是说，检测室是医疗器械制造企业的一部分，而所有与器械相关的部门均应遵守质量体系规章。
That is, the test laboratory is simply a part of a medical device manufacturer of which all device-related divisions shall comply with the QS regulation.
也就是说，检测室是医疗器械制造企业的一部分，而所有与器械相关的部门均应遵守质量体系规章。
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