11.040.20 输血、输液和注射设备 标准查询与下载
共找到 1427 条与 输血、输液和注射设备 相关的标准，共 96 页
Infusion equipment for medical use－Part 11：Infusion filters for use with pressure infusion equipment
- ICS
- 11.040.20
- CCS
- 发布
- 2017-09-29
- 实施
Elastomeric parts for parenterals and for devices for pharmaceutical use－Part 2：Identification and characterization
- ICS
- 11.040.20
- CCS
- 发布
- 2017-09-29
- 实施
Infusion equipment for medical use－Part 9：Fluid lines for use with pressure infusion equipment
- ICS
- 11.040.20
- CCS
- 发布
- 2017-09-29
- 实施
Infusion equipment for medical use－Part 10：Accessories for fluid lines for use with pressure infusion equipment
- ICS
- 11.040.20
- CCS
- 发布
- 2017-09-29
- 实施
Infusion equipment for medical use－Part 12：Check valves
- ICS
- 11.040.20
- CCS
- 发布
- 2017-09-29
- 实施
Medical devices. Pump tube spallation test. General procedure
- ICS
- 11.040.20
- CCS
- 发布
- 2017-09-13
- 实施
- 2017-09-30
Standard Guide for Characterization and Presentation of the Dimensional Attributes of Vascular Stents
- ICS
- 11.040.20
- CCS
- 发布
- 2017-09-01
- 实施
Standard Test Method for Measuring Intrinsic Elastic Recoil of Balloon-Expandable Stents
- ICS
- 11.040.20
- CCS
- 发布
- 2017-09-01
- 实施
Standard Guide for Measuring Securement of Balloon Expandable Vascular Stent Mounted on Delivery System
- ICS
- 11.040.20
- CCS
- 发布
- 2017-09-01
- 实施
Single-use containers for human venous blood specimen collection
- ICS
- 11.040.20
- CCS
- 发布
- 2017-09-01
- 实施
This part of ISO 8536 specifies the shape, dimensions, material, performance requirements and labelling for the type of closure for infusion bottles, as described in ISO 8536-1, that is used in connection with the freeze-drying (or lyophilization) of drugs and biological materials. The dimensional requirements are not applicable to barrier-coated closures. Closures specified in this document are intended for single use only. Freeze drying closures can pick up water during shipping, storage, washing and steam sterilization cycles, which is difficult to remove in a subsequent drying cycle. As a consequence, the freeze drying closures are usually loaded with residual moisture. Depending upon the mass of the freeze-dried product and the degree of its sensitivity to water, the residual moisture in the rubber material can spoil the freeze-dried preparation during storage. These specific process requirements have been addressed in this part of ISO 8536 by specifying relevant requirements for freeze drying closures including a test method on determination of residual moisture.
Infusion equipment for medical use - Part 6: Freeze drying closures for infusion bottles (ISO 8536-6:2016)
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-09-00
- 实施
Medical devices — Pump tube spallation test — General procedure
- ICS
- 11.040.20
- CCS
- 发布
- 2017-08-17
- 实施
Intravascular Catheters Single Use Sterile Catheters Part 3: Central Venous Catheters
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-07-17
- 实施
- 2019-01-01
Intravascular Catheters Single Use Sterile Catheters Part 4: Balloon Dilatation Catheters
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-07-17
- 实施
- 2019-01-01
Single-use autologous blood processing equipment Part 1: Centrifugal cup-type blood cell recovery device
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-07-17
- 实施
- 2018-07-01
This document specifies requirements and test methods for evacuated and non-evacuated single-use venous blood specimen containers. It does not specify requirements for blood collection needles, needle holders, blood culture receptacles or “arterial” blood gas collection devices that can be used for venous blood.
Single-use containers for human venous blood specimen collection
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-07-01
- 实施
Transfusion equipment for medical use - Part 3: Blood-taking sets for single use (ISO 1135-3:2016); German version EN ISO 1135-3:2017
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-05
- 实施
Methods for testing particulate contamination of medical infusion, blood transfusion, and injection equipment
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-03-28
- 实施
- 2018-04-01
Standard test model for evaluation of surface sliding properties of non-intravascular catheters
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-03-28
- 实施
- 2018-04-01
本标准规定了医用血浆病毒灭活箱(以下简称病毒灭活箱)的通用要求、试验方法、检验规则、标志和使用说明书、包装等。 本标准适用于与符合YY 0765.1规定的病毒灭活器材配合使用的医用血浆病毒灭活箱。
Medical plasma virus inactivated device
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-03-28
- 实施
- 2018-04-01
