发布时间:2024-05-27 17:49:26 - 更新时间:2024年06月29日 15:22
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Przedmiotem normy s? szczypczyki anatomiczne do szwu naczyniowego, u?ywane przy zabiegach chirurgicznych
基于当前医学知识水平,YY/T 0663的本部分明确了对血管内假体的各种要求。关于安全方面,本部分在预期性能、设计属性、材料、设计评价,制造、灭菌包装及制造商提供的信息方面提出了要求。YY/T 0640规定了源外科植入物性能的通用要求,本部分宜视为对YY/T 0640的补充。本部分适用于治疗动脉瘤
Cardiovascular implant.Endovascular devices.Part 1:Endovascular prostheses
この規格は,心臓及び脈管をX線写真で検査するため,造影剤を心臓,大血管及び冠動脈に注入する際に用いる血管遺影用活栓,造影用耐圧チュープ及び針なし造影用輸液セットから構成するもの(以下,血管造影用セットという。)について規定する
Angiographic set
This part of ISO 25539 specifies requirements for vascular stents, based upon current medical knowledge. With regard to safety, it gives requirements
Cardiovascular implants - Endovascular devices - Part 2: Vascular stents
Cardiovascular implants — Endovascular devices — Part 2: Vascular stents
Cardiovascular implants — Endovascular devices — Part 2: Vascular stents
Cardiovascular implants. Endovascular devices. Part 2. Vascular stents
Calibration Specification for Hemodialysis Equipment Tester
Cardiovascular implants — Endovascular devices — Part 4: Application of ISO 17327-1 for coated endovascular devices
Cardiovascular implants — Endovascular devices — Part 4: Application of ISO 17327-1 for coated endovascular devices
Cardiovascular implants - Endovascular devices - Part 1 : endovascular prostheses.
This part of ISO 25539 specifies requirements for endovascular prostheses, based upon current medical knowledge. With regard to safety, it gives
Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (Incorporating corrigendum February 2011)
Cardiovascular implants. Endovascular devices. Part 1. Endovascular prostheses
本标准规定了海水淡化装置用铜合金缝管的要求、试验方法、检验规则和包装、标志、运输、贮存及订货单(或合同)内容等。 本标准适用于海水淡化及其他脱盐装置用铜合金缝管
Seamless copper alloy tube for water desalting applications
Przedmiotem normy s? szczypczyki do szwu naczyniowego, u?ywane przy zabiegach chirurgicznych
Specifies requirements for endovascular prostheses, based upon current medical knowledge. With regard to safety, it gives requirements for intended
Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses
The General Services Administrations has authorized the use of this commercial item description
CATHETERIZATION SET, CARDIOVASCULAR
Shall beasteril , disposable administration or pooling "YI' set fortransfusing blood platelets. The administration-pooling set shall consist of a "Yl
BLOOD PLATELET ADMINISTRATION-POOLING SET
Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 2: Local regulatory information
Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products
Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products
The Amendment provides guidance for the development of preclinical test methods to be used to characterize and evaluate endovascular prostheses
Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses, Amendment 1: Test methods
The catheter set shall be a sterile, disposable, 20 gauge by 1-3/4 inches (4.45 cm), radiopaque,polytetrafluoroethylene catheter over a 22 gauge, thin
CATHETERIZATION SET, CARDIOVASCULAR, RADIAL ARTERY
Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 2: Local regulatory information
本标准规定了与血液透析器、血液透析滤过器等血液净化装置配合使用的一次性使用的体外循环血路(以下简称体外循环血路)及传感器保护器(-体型和分离器)的技术要求、试验方法以及标志说明。 本标准不适用于: —血液透析器、血液透析滤过器或血液滤过器; —血浆分离器; —血液灌流器; —血管通路装置
Cardiovascular implants and artificial organs.Extracorporeal blood circuit for blood purification devices
The cuff shall be a blood warming cuff used in enclosing blood or parenteral fluids for heating during intravenous transfusion procedures. The blood
CUFF, BLOOD WARMER
This standard establishes labeling and performance requirements, test methods, and terminology that will help define a reasonable level of safety
Autologous transfusion devices
この規格は,保存血液など血液製剤を輸血するための滅菌済み輸血セット(以下,輸血セットという。)で,そのまま直ちに使用でき,かつ,1回限りの使用で使い捨てる輸血セットの要求事項について規定する
Sterile blood transfusion set
Sterile blood transfusion set
This document has been prepared to provide minimum requirements for vascular stents. The normative requirements are provided in the main body
Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2020); German version EN ISO 25539-2:2020