一、关于 FDA 510 ( K )
世界范围内对医疗器械需求量的不断增大,为众多医疗器械制造商提供了极好机遇。但想进入相关市场,就必须遵循当地的管理法令、法规和标准。要进入美国市场,就必须通过FDA的相关审核。
根据美国医疗器械分类标准,医疗器械分类以“对产品的控制程度为基础”,为确保医疗器械产品的安全性,分为“基本”控制和“特殊”控制。医疗器械产品可分为 I 类、II类和III类,根据FDA的数据统计,目前,大约I类产品的7%,II类产品的92%,III类产品的80%通常选择FDA510 ...
CUC may grant exemptions from the annual On-Site Audit cycle for Traders (with or without physical possession) identified as low risk. In this case, a desk audit may be conducted to replace the on-site verification or may exempt from the Certificatio ...
5.0 Managing verified claimed product during production 在生产过程中管理经过验证的认证产品
5.1 The Organization shall demonstrate control over the flow of products within the unit. e.g. processing/
manufacturing steps performed), recipes used, composition, and stoc ...
1.1 Verifications Requirements 验证要求
Verification Protocol applies to each Organization in the full supply chain (after the verification of the source Claimed Material), including processing, manufacturing, storage, handling and shipping through to ...