Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling U.S. FDA Guidance, Document issued on: March 17, 2015检测

电议

再处理验证 Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling U.S. FDA Guidance, Document issued on: March 17, 2015

检测项目

再处理验证

Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling U.S. FDA Guidance, Document issued on: March 17, 2015-

支持报告类型：电子报告、纸质报告

支持报告语言：中文报告、英文报告、中英文报告

报告盖章资质： CMA；CNAS

服务周期： 3-10个工作日（特殊样品除外）

服务地区：全国

检测用途：电商平台入驻；商超卖场入驻；产品质量改进；产品认证；出口通关检验等

取样方式：快递邮寄或上门取样

样品要求：样品数量及规格等视检测项而定

服务详情

检测标准

检测项目再处理验证

检测标准号 U.S. FDA Guidance, Document issued on: March 17, 2015

检测方法名 Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling U.S. FDA Guidance, Document issued on: March 17, 2015

限制说明

服务简介

服务范围：GB、GB/T、FZ/T品控检测、各类电商平台、商超卖场入驻质检。

服务流程

合作机构资质

报告样例

平台优势

百检介绍

相关标准

《U.S. FDA 21 CFR 175.300(e) U.S. FDA 21 CFR 177.1900》树脂和聚合物的涂料（条款e: 分析方法）用于模制制品的脲醛树脂 U.S. FDA 21 CFR 175.300(e) U.S. FDA 21 CFR 177.1900
《U.S. FDA 21CFR 177.1550》全氟烃树脂 U.S. FDA 21CFR 177.1550
《AAMI TIR12:2010》Designing, testing, and labeling reusable medical devices for reprocessing in health care facilities: A guide for medical device manufacturers AAMI TIR12:2010
《U.S. FDA 21CFR 177.1520》烯烃聚合物 U.S. FDA 21CFR 177.1520
《ASTM F3208-20》Standard Guide for Selecting Test Soils for Validation of Cleaning Methods for Reusable Medical Devices ASTM F3208-20
《U.S. FDA 21CFR 177.1670》聚乙烯醇薄膜 U.S. FDA 21CFR 177.1670
《U.S. FDA 21 CFR 177.1580》聚碳酸酯树脂 U.S. FDA 21 CFR 177.1580
《U.S. FDA 21 CFR 177.1500》尼龙树脂 U.S. FDA 21 CFR 177.1500
《U.S. FDA Guidance, Document issued on: March 17, 2015》Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling U.S. FDA Guidance, Document issued on: March 17, 2015
《U.S. FDA 21CFR 177.2470》聚甲醛共聚物 U.S. FDA 21CFR 177.2470

电话咨询

扫码优惠

我要检测