IEC 60601-2-52:2009/COR1:2010

IEC 60601-2-52:2009/COR1:2010 provides a corrigendum to Corrigendum 1 - Medical electrical equipment - Part 2-52: Particular requirements for the basic safety and essential performance of medical beds, helping users apply the parent document more accurately in engineering and compliance work. It is relevant for organizations that rely on documented evaluation, risk management, and technical review when assessing medical beds for safety and essential performance. For procurement, testing, and regulatory preparation, IEC 60601-2-52:2009/COR1:2010 supports a cleaner compliance reference tied to the original 2009 publication.

IEC 60601-2-52:2009/COR1:2010 standard overview

This corrigendum is a supporting document connected to IEC 60601-2-52:2009, rather than a standalone technical specification. Its purpose is to correct or clarify the parent text for medical beds covered under the requirements for basic safety and essential performance. In practice, that makes it useful during technical assessment, conformity assessment, and quality workflows where exact wording matters. Organizations often use it to maintain consistency across engineering documentation, verification activities, and compliance preparation tied to the original publication.

Applications of IEC 60601-2-52:2009/COR1:2010

IEC 60601-2-52:2009/COR1:2010 is typically used by manufacturers, test laboratories, and compliance teams working with medical beds and related electrical equipment documentation. It may be referenced during product evaluation, design review, and laboratory evaluation when teams need to confirm that the parent requirements are being applied correctly. It is also useful in procurement and regulatory workflows where a corrected compliance reference helps reduce interpretation differences between engineering, testing, and certification stakeholders.

Why IEC 60601-2-52:2009/COR1:2010 matters

Supporting documents like this corrigendum matter because small textual corrections can affect safety evaluation, test interpretation, and the consistency of conformity assessment records. For medical beds, clear requirements help teams align verification activities with essential performance expectations and reduce avoidable compliance risk. IEC 60601-2-52:2009/COR1:2010 can therefore be important in operational quality assurance, technical validation, and regulatory preparation, especially when a project needs a reliable source for engineering decisions and documentation control.

• Corrective reference linked to the parent medical bed safety document
• Useful for technical review, verification activities, and documented evaluation
• Supports compliance workflows and conformity assessment preparation
• Helps maintain consistency in engineering documentation and test interpretation
• Relevant to procurement teams validating the exact compliance reference in use