IEC 60336:2020/COR1:2022
Corrigendum 1 - Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Focal spot dimensions and related characteristics
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About This Item
IEC 60336:2020/COR1:2022 is a corrigendum linked to IEC 60336:2020, addressing Corrigendum 1 - Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Focal spot dimensions and related characteristics. It is relevant for organizations that rely on documented technical accuracy in medical X-ray equipment evaluation, especially where focal spot dimensions and related characteristics affect design review, verification activities, and conformity assessment. In procurement and compliance workflows, IEC 60336:2020/COR1:2022 helps ensure that references to the parent document remain technically aligned and suitable for controlled documentation use.
Overview of IEC 60336:2020/COR1:2022
This corrigendum serves as a supporting technical document for IEC 60336:2020, rather than a standalone testing standard. Its role is to correct or clarify content associated with medical electrical equipment used in X-ray tube assemblies for medical diagnosis, with particular attention to focal spot dimensions and related characteristics. For engineering and quality teams, that makes it useful during technical review, documented evaluation, and specification control when maintaining accurate requirements for product assessment, verification, and compliance reference management.
Compliance applications of IEC 60336:2020/COR1:2022
IEC 60336:2020/COR1:2022 may be used in laboratory evaluation, regulatory preparation, and product documentation workflows where the parent reference is being applied to medical diagnostic X-ray tube assemblies. It is especially relevant when teams are checking technical consistency across design files, test plans, and procurement records. In practice, it can support conformity assessment activities by helping maintain precise references for performance-related characteristics and by reducing the risk of using outdated or uncorrected technical wording in compliance submissions.
Importance of compliance with IEC 60336:2020/COR1:2022
Using IEC 60336:2020/COR1:2022 in controlled documentation helps improve technical accuracy, which is important for safety, verification consistency, and risk management in medical electrical equipment workflows. For manufacturers, test laboratories, and procurement teams, corrigenda can affect engineering validation and conformity assessment preparation by ensuring the parent document is interpreted correctly. This supports operational consistency across quality systems, reduces ambiguity in compliance workflows, and helps maintain a reliable basis for product evaluation and regulatory review.
- Supporting corrigendum tied to IEC 60336:2020 for controlled technical use
- Relevant to focal spot dimensions and related characteristics of medical X-ray tube assemblies
- Useful for engineering documentation, test planning, and compliance review
- Helps maintain accurate references during conformity assessment and quality workflows
- Publication Date: 2022-06-21
- Standard Status: Corrigendum
- Publisher: IEC
- Edition: 5
- This Version: IEC 60336:2020 (2022-06-21)
- Previous Version: IEC 60336:2020 (2020-12-17)
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