100 标准查询与下载

SY/T 6118-2013 热力釆油蒸汽发生器水处理系统运行技术规程

本标准规定了稠油热力采油蒸汽发生器水处理系统(以下简称水处理)的运行技术要求、软化器运行参数与整定方法、化验分析要求及健康、安全、环境控制要求。本标准适用于油田用热力采油蒸汽发生器配套的具有软化和除氧功能的水处理系统。

The technical specifications for water processing system operation of thermal recovery steam generator

DS/ISO 9999:1992 残疾人技术辅助器具．分类

This International Standard establishes a classification of technical aids for disabled persons and can be used in conjunction with information systems. For the time being, it is restricted to those technical aids which are mainly used individually. In special cases, parts, accessories and adaptations are classified separately. Technical aids for public traffic and accessibility in buildings are not dealt with, but will be incorporated later. The following items are excluded from this International Standard: — items used for the installation of technical aids; — solutions obtained by combinations of technical aids which are classified elsewhere; — medicines; — technical aids and instruments, exclusively used in medical practice; — training for handling the aids; — financial support.

Technical aids for disabled persons. Classification

DS/ISO 7864:1991 一次性使用无菌皮下注射针头

This International Standard specifies requirements for sterile hypodermic needles for single use.

Sterile hypodermic needles for single use

DS/ISO 6009:1991 一次性使用皮下注射针.识别用的色标

This International Standard establishes a colour code for the identification of hypodermic needles for single use, the hubs of which are made of plastics material. This International Standard can also be used for a needle the hub of which is made of other materials. The colour coding is equally applicable to thin-walled needles. In all cases the colour indicates the external diameter.

Hypodermic needles for single use. Colour coding for identification

DS/ISO 8537:1991 胰岛素用有或无针头一次性无菌注射器

This International Standard specifies requirements and test methods for sterile syringes with or without needles intended for single use solely for the in-jection of insulin and primarily in humans. It covers syringes for use with 40 units of insulin/ml (U-40) and 100 units of insulin/ml (U-100). Sterile syringes specified in this International Stan-dard are intended for use soon after filling as they are not suitable for containing insulin over extended periods of time.

Sterile single-use syringes, with or without needle, for insulin

DS/ISO 5359:1990 医疗气体系统用的低压、易弯连接部件(软管部件)

This International Standard specifies requirements for hose assemblies for use with medical gas supply systems for clinical applications. Requirements are given for the design, performance, identifi-cation and testing of hose assemblies used for conveying the medical gases listed in table 1. Hose assemblies with connectors as defined in 3.7, 3.8, 3.9 and 3.10 and as illustrated in figure 1, are intended for use in the following situations: a) between a pipeline terminal unit and medical equipment (see figure 2); b) between the fixed pipeline system and a terminal unit of that system at which the user makes connections and disconnections (see figure 3); c) between a terminal unit at the end of the fixed pipeline system and a second terminal unit or a quick-connector socket (see figure 4); d) for connection between an emergency supply and a fixed pipeline system (see figure 5); e) for connection between a medical gas pressure regulator and medical equipment. Certain types of equipment contain internally installed hose assemblies which cannot be removed by the user, or maintained without dismantling the equipment, e.g. overhead pendant tracks and some hinged arm booms (see figure 6). These are not included in the scope of this International Standard. This International Standard does not include requirements for electrical conductivity.

Low pressure flexible connecting assemblies (hose assemblies) for use with medical gas systems

DS/ISO 595-1:1989 可重复使用的全玻璃或金属-玻璃医用注射器.第1部分:尺寸

This part of ISO 595 specifies dimensions for reusable all-glass or metal-and-glass syringes for medical use, having a graduated capacity from 1 to 100 ml. It also specifies requirements for the graduated capacity of syringes. ISO 595/2 specifies the design, the performance requirements and the corresponding test methods for reusable syringes. NOTE — The term "all-glass syringe" relates to syringes with a barrel and piston made entirely of glass, with either a glass or a metal nozzle. The term "metal-and-glass syringe" relates to syringes with a glass barrel, a metal nozzle and a piston which may be either metal or partially metal.

Reusable all-glass or metal-and-glass syringes for medical use. Part 1: Dimensions

DS/ISO 5356-1:1989 麻醉剂和呼吸设备.锥形连接器.第1部分:锥体和插孔

This part of ISO 5356 specifies basic dimensional and gauging requirements for cones and sockets intended for use in breathing systems, anaesthetic gas scavenging systems and vaporizers. NOTE — Requirements for screw-threaded weight-bearing conical connectors are specified in ISO 5356-2.

Anaesthetic and respiratory equipment. Conical connectors. Part 1: Cones and sockets

DS/ISO 5362:1989 麻醉剂储存袋

This International Standard specifies requirements for reservoir bags for use with anaesthetic or breathing apparatus. It is con-cerned with the design of the neck, size designation, com-pliance and, where relevant, requirements for electrical con-ductivity. Special purpose bags, for example bellows and self-expanding bags, are excluded from the scope of this International Standard.

Anaesthetic reservoir bags

DS/ISO 5364:1989 口咽导气管

This International Standard specifies the size designation and certain basic requirements for oropharyngeal airways which may include but are not limited to the following types : - Guedel's - Phillip's - Water's

Oropharyngeal airways

DS/ISO 594-1:1989 注射器、针头和某些其它医用设备的有6% 锥度的锥形配件.第1部分:一般要求

This part of ISO 594 specifies requirements for conical fittings with a 6 % (Luer) taper for use with hypodermic syringes and needles and with certain other apparatus for medical use such as transfusion and infusion sets. It covers conical fittings made of rigid and of semi-rigid materials and includes test methods for gauging and performance. It excludes provision for more flexible or elastomeric materials. Figure 1 illustrates typical male 6 % (Luer) conical fitting ("male fitting") and female 6 % (Luer) conical fitting ("female fitting"). NOTE — It is not practicable to define the characteristics of rigid or semi-rigid materials with precision, but glass and metal may be con-sidered as typical rigid materials. By contrast, many plastic materials may be regarded as semi-rigid although the wall thickness is an important factor influencing the rigidity of a component.

Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment. Part 1: General requirements

DS/ISO 7767:1989 监控病人呼吸混合物的氧分析仪.安全要求

ISO 7767 is one of a series of International Standards based on IEC 601-1 : 1977; in IEC 601-1 : 1977 (the "General Standard"), this type of International Standard is referred to as a "Particular Standard". As stated in 1.3 of IEC 601-1 : 1977, the requirements of this International Standard take precedence over those of IEC 601-1 : 1977. The scope and object given in clause 1 of IEC 601-1 : 1977 applies except that 1.1 shall be replaced by the following. This International Standard specifies safety requirements for oxygen analyzers, as defined in 3.8 (in this International Standard) intended for use in determining the oxygen level in breathing gas mixtures administered to patients. Both sampling and non-sampling oxygen analyzers are covered. The field of application includes, but is not limited to, a) anaesthetic machines and breathing systems; b) ventilators; c) baby incubators; d) oxygen concentrators (domiciliary or clinical). Oxygen analyzers intended for use in laboratory research applications are outside the scope of this International Standard.

Oxygen analyzers for monitoring patient breathing mixtures. Safety requirements

DS/ISO 8185:1989 医用增湿器. 安全要求

ISO 8185 is one of a series of International Standards based on IEC Publication 601-1; in IEC Publication 601-1 (the "General Standard"), this type of International Standard is referred to as a "Particular Standard". As stated in 1.3 of IEC Publication 601-1, the requirements of this International Standard take precedence over those of IEC Publication 601-1. Humidifiers may be gas-powered, electrically powered or both. However, this International Standard has been prepared as a Particular Standard based on IEC Publication 601-1, which gives general requirements for all aspects of safety, not only electrical safety, and many of the requirements are therefore applicable to humidifiers not powered by electricity. Where this International Standard specif ies that a clause of IEC Publication 601-1 applies, it means that the clause applies only if the requirement is relevant to the humidifier under consideration. The scope and object given in clause 1 of IEC Publication 601-1 applies except that 1.1 shall be replaced by the following: This International Standard specifies requirements for the safety of vaporizing and nebulizing humidifiers, including those suitable for inclusion in breathing systems, for use with both intubated and non-intubated patients. This International Standard also includes requirements for delivery tubes and accessory devices intended to control humidifier or delivery tube heaters. Devices commonly referred to as "room humidifiers" and humidifiers used in heating, ventilation and air conditioning systems are outside the scope of this International Standard. Requirements for heat and moisture exchangers are given in ISO 9360 (in preparation).

Humidifiers for medical use. Vaporizers and nebulizers. Safety requirements

DS/ISO 8382:1989 用于人的复苏器

This International Standard specifies minimum performance and safety requirements for ventilatory resuscitators intended for use with all age groups. It specifies the performance of operator-powered and gas-powered ventilatory resuscitators which are portable and intended for use in emergency situ-ations to provide lung ventilation to individuals whose breathing is inadequate. For gas-powered resuscitators, re-quirements are included for the gas supply. Resuscitators for infants and children are designated according to body mass range and approximate age equivalent. Devices which have been designed only to deliver gases to a patient breathing adequately and devices which are intended to assist or provide for the ventilation of a patient for an extended period of time are not covered by this International Standard. Electrically-powered resuscitators are not covered by this Inter-national Standard.

Resuscitators intended for use with humans

DS/ISO 8669-2:1989 尿收集袋. 第2部分: 尺寸的测定

This part of ISO 8669 specifies methods for determining the dimensions of urine collection bags. The purpose is to measure dimensions related to the end use of the products. Dimensions given in this International Standard are for iden-tification purposes only and do not individually or collectively define or recommend a product of a specific design, style or size.

Urine collection bags. Part 2: Determination of dimensions

DS/ISO 8836:1989 用于呼吸道的吸气引液导管

This International Standard specifies requirements for suction catheters intended for use in suction of the respiratory tract. It covers suction catheters that are supplied either sterile or non-sterile and those that are intended either for single use or to be reused.

Suction catheters for use in respiratory tract

DS/ISO 5361-1:1987 导气管.第1部分:一般要求

This part of ISO 5361 specifies general requirements for tracheal (endotracheal) tubes.

Tracheal tubes. Part 1: General requirements

DS/ISO 5361-5:1987 导气管.第5部分:套箍和软管的试验要求和方法

This part of ISO 5361 specifies requirements for a manufac-turer's type test, i.e. to be carried out on new unused tubes for the evaluation of tube collapse and cuff herniation of cuffed tracheal tubes.

Tracheal tubes. Part 5: Requirements and methods of test for cuffs and tubes

DS/ISO 7376-1:1987 喉镜检查器.第1部分:钩接式有柄刀片装置

This part of ISO 7376 specifies basic dimensions for the parts of the joint between any blade and any handle of a hook-on type laryngoscope, used mainly for tracheal intubation, in which an electric lamp in the blade is supplied with power through the handle. The fittings specified provide for both mechanical fixation and for completion of the electrical circuits from the handle to the blade and lamp. Part 2 of ISO 7376 specifies screw-threads for electric lamps and lamp sockets.

Laryngoscopic fittings. Part 1: Hook-on type handle-blade fittings

DS/ISO 7376-2:1987 喉镜检查器.第2部分:微型电灯.螺纹和插座

This part of ISO 7376 specifies requirements for screw threads for miniature electric lamps and lamp sockets used in laryngoscopes as described in part 1 of this International Standard. The contact form and general dimensions of these lamps are also specified.

Laryngoscopic fittings. Part 2: Miniature electric lamps. Screw threads and sockets