IVDD技术文件内容
Contents of TechnicalDocumentation
技术文件内容
Acc. to Annex I & III of IVDD98/79/EC按体外诊断医疗器械指令附录III
Contents | 内容 | |
1. | Table of content | 目录 |
2. 2.1 2.2 2.3 2.4 2.5 | General Information Manufacturer European Representative Short general description of the product Location of – design, -manufacturing facilities In case of contract design / manufacturing/sterilization | 一般信息 厂商 欧洲代表 产品的简短描述 设计、生产场地 设计/生产/消毒的分承包方
|
3 3.1 3.2 3.3 3.4 3.5 3.6 3.7 3.8 3.9
| Product description Product family description Accessories Intended use Categorization Conformity assessment route Notified body Applicable standards Declaration of conformity Quality system certificate, approvals etc. | 产品描述 产品组描述 附件 预期用途 分类 符合性评审路径 公告机构 适用的标准 符合性声明 质量体系证书,批准等等 |
4 4.1 4.2 4.3 4.4
| 4.1 Product 4.2 Compliance with essential requirements 4.3 Risk Analysis Manufacturing Process Packaging specifications
| 产品 符合基本需求 风险分析 生产过程 包装规格 |
5 5.1 5.2 5.3 5.4 5.5 5.6 5.7
| PRODUCT VERIFICATION Stability studies Performance evaluation studies For self testing devices Reference material, calibration and control materials Safety testing Software validation QC / QA processes
| 产品确认 稳定性研究 性能评估研究 自我测试器械 参考材料,校准和对照材料 安全测试 软件验证 QC/QA 过程 |
6 6.1 6.2 | LABELING AND INSTRUCTION FOR USE Labels Instruction for use | 标签和使用说明书 标签 使用说明书 |
7 | LITERATURE, PUBLICATIONS
| 文献,出版物 |
5.1 8 | REVISION HISTORY OF THE TECHNICAL FILE
| 技术文件的修订记录 |