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
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
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing (ISO 8871-5:2016); German version EN ISO 8871-5:2016
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-03
- 实施
Disposable high-pressure contrast syringes and accessories
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-02-28
- 实施
- 2018-01-01
Transfusion equipment for medical use. Blood-taking sets for single use
- ICS
- 11.040.20
- CCS
- C47;C31
- 发布
- 2017-02-28
- 实施
- 2017-02-28
Air filters for infusion and blood transfusion equipment Part 3: Integrity test methods
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-02-28
- 实施
- 2018-01-01
Air filters for infusion and blood transfusion equipment - Part 2: Test methods for bacterial retention in liquids
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-02-28
- 实施
- 2018-01-01
Guidelines for Compatibility Study of Disposable Infusion Devices and Drugs Part 1: Drug Adsorption Study
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-02-28
- 实施
- 2018-01-01
Transfusion equipment for medical use - Part 3: Bloodtaking sets for single use
- ICS
- 11.040.20
- CCS
- G50
- 发布
- 2017-02
- 实施
Infusion equipment for medical use. Freeze drying closures for infusion bottles
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-01-31
- 实施
- 2017-01-31
Infusion equipment for medical use - Part 13: Graduated flow regulators for single use with fluid contact (ISO 8536-13:2016); German version EN ISO 8536-13:2016
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2017-01
- 实施
Medical devices. General safety and compatibility requirements for single use infusion sets
- ICS
- 11.040.20
- CCS
- 发布
- 2017-00-00
- 实施
- 2018-07-01
DIN EN ISO 8362-1:2017 注射容器和附件. 第1部分：玻璃管制成的注射小瓶(ISO / DIS 8362 - 1:2017)；德文和英文版本prEN ISO 8362-1:2017
This document specifies the form, dimensions and capacities of glass vials for injectable preparations. It also specifies the material from which such containers are made of and the performance requirements of those containers. This document applies to colourless or amber glass containers made from borosilicate or soda-lime glass, made from glass tubing, whether internally surface-treated or not, and intended to be used in the packaging, storage or transportation of products intended for injection.
Injection containers and accessories - Part 1: Injection vials made of glass tubing (ISO/DIS 8362-1:2017); German and English version prEN ISO 8362-1:2017
- ICS
- 11.040.20
- CCS
- 发布
- 2017
- 实施
Medical devices. Syringe pumps. Technical requirements for governmental purchases
- ICS
- 11.040.20
- CCS
- 发布
- 2017
- 实施
- 2018-06-01
Infusion equipment for medical use - Part 6: Freeze drying closures for infusion bottles
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2016-12-00
- 实施
Small-bore connectors for liquids and gases in healthcare applications. Connectors for limb cuff inflation applications
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2016-11-30
- 实施
- 2016-11-30
Elastomeric parts for parenterals and for devices for pharmaceutical use. Functional requirements and testing
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2016-11-30
- 实施
- 2016-11-30
Small-bore connectors for liquids and gases in healthcare applications - Part 5: Connectors for limb cuff inflation applications
- ICS
- 11.040.20
- CCS
- 发布
- 2016-11-01
- 实施
Infusion equipment for medical use - Part 14: Clamps and flow regulators for transfusion and infusion equipment without fluid contact
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2016-11-00
- 实施
Transfusion equipment for medical use - Part 3: Blood-taking sets for single use
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2016-11
- 实施
Dieser Teil von ISO 8871 legt Anforderungen und Prüfverfahren hinsichtlich funktioneller Merkmale von Verschlüssen aus Elastomeren fest, die für Injektionsflaschen verwendet und mit einer Injektionskanüle durchstochen werden. ANMERKUNG Funktionelle Prüfungen unter Verwendung von Dornen sind in ISO 8536-2 und ISO 8536-6 festgelegt.
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing
- ICS
- 11.040.20
- CCS
- C14
- 发布
- 2016-11
- 实施
