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
Transfusion equipment for medical use ―Part 3: Blood-taking sets for single use
- ICS
- 11.040.20
- CCS
- 发布
- 2020-12-30
- 实施
Caps made of aluminium-plastics combinations for infusion bottles and injection vials — Requirements and test methods
- ICS
- 11.040.20
- CCS
- 发布
- 2020-12-30
- 实施
Transfusion equipment for medical use ―Part 4: Transfusion sets for single use, gravity feed
- ICS
- 11.040.20
- CCS
- 发布
- 2020-12-30
- 实施
本文件规定了非电驱动一次性使用便携式输注泵（以下简称输注泵）的术语和定义、基本要求、组成、技术要求、试验方法、检验规则、标志、包装、运输及贮存和质量承诺。 本文件适用于可持续给液、带或不带自主控制给液的输注泵。 本文件不适用于： a) IEC 60601-2-24 所包括的电驱动或电控制的输注泵； b) 植入式装置； c) 肠给养泵； d) 经皮给液装置； e) 输液动力不是装置自身提供动力，而是通过患者主动干预来获得动力（如：只靠重力作为动力的装置）。
Portable infusion devices for single use-Non electrically driven
- ICS
- 11.040.20
- CCS
- C358
- 发布
- 2020-12-30
- 实施
- 2021-02-08
Injection equipment for medical use — Part 2: One-point-cut(OPC) ampoules
- ICS
- 11.040.20
- CCS
- 发布
- 2020-12-30
- 实施
Infusion equipment for medical use — Part 5: Burette infusion sets for single use, gravity feed
- ICS
- 11.040.20
- CCS
- 发布
- 2020-12-30
- 实施
Infusion equipment for medical use — Part 6: Freeze drying closures for infusion bottles
- ICS
- 11.040.20
- CCS
- 发布
- 2020-12-30
- 实施
Injection containers and accessories — Part 7: Injection caps made of aluminium-plastics combinations without overlapping plastics part
- ICS
- 11.040.20
- CCS
- 发布
- 2020-12-30
- 实施
Injection equipment for medical use — Part 1: Ampoules for injectables
- ICS
- 11.040.20
- CCS
- 发布
- 2020-12-30
- 实施
Aluminium caps for transfusion, infusion and injection bottles — General requirements and test methods
- ICS
- 11.040.20
- CCS
- 发布
- 2020-12-30
- 实施
Caps made of aluminium-plastics combinations for infusion bottles and injection vials — Requirements and test methods
- ICS
- 11.040.20
- CCS
- 发布
- 2020-12-30
- 实施
Technical specifications for clinical blood use in medical institutions
- ICS
- 11.040.20
- CCS
- C27
- 发布
- 2020-12-24
- 实施
- 2021-04-01
Elastomeric parts for parenterals and for devices for pharmaceutical use -- Part 2: Identification and characterization (ISO 8871-2:2020)
- ICS
- 11.040.20
- CCS
- 发布
- 2020-12-14
- 实施
- 2020-12-14
本标准主要从试验模型、试验方法、试验结果分析、报告等方面，规定了带有亲水涂层导尿管的涂层润滑性和润滑稳定性的测试和评价。
Lubrication performance evaluation method for urethral catheter hydrophilic coating
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2020-12-13
- 实施
- 2021-03-01
Medical devices. Non-electrically driven portable infusion devices
- ICS
- 11.040.20
- CCS
- 发布
- 2020-11-12
- 实施
- 2020-11-12
Elastomeric parts for parenterals and for devices for pharmaceutical use. Determination of released-particle count
- ICS
- 11.040.20
- CCS
- 发布
- 2020-11-12
- 实施
- 2020-11-12
本文件规定了医用一次性使用聚醚砜微孔滤膜（以下简称滤膜）的术语和定义、基本要求、产品型号说明和分类、技术要求、试验方法、检验规则、标志、包装、运输、贮存和质量承诺。 本文件适用于标称孔径 0.22 μm～20 μm 的滤膜。
Single-use polyethersulfone microporous membrane for medical device
- ICS
- 11.040.20
- CCS
- C358
- 发布
- 2020-11-11
- 实施
- 2020-11-19
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2020)
- ICS
- 11.040.20
- CCS
- 发布
- 2020-11-00
- 实施
- 2020-11-01
Disposable intravenous nutrition infusion bag
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2020-09-27
- 实施
- 2021-09-01
Determination of compatibility of blood transfusion sets and blood components Part 2: Assessment of blood component damage
- ICS
- 11.040.20
- CCS
- C31
- 发布
- 2020-09-27
- 实施
- 2021-09-01
