Reference details
- Reference
- EN IEC 60601-2-22:2020/A11:2026
- Official title
- Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment
- Organisation
- CENELEC
- Publisher status in source
- PublishedThis is the status recorded in the source, not a statement that this is the latest edition.
- Source access
- 19 October 2026
Research and application
Begin with the official scope and the product configuration. The title identifies a subject; it does not establish every product, use condition or legal requirement covered by the publication.
Product research routes
- Lighting and optical products
Light sources, luminaires, control gear and optical functions, with separate treatment of product and installation evidence.
- Medical devices
Intended medical purpose, device classification and the evidence associated with design, performance and lifecycle controls.
- In vitro diagnostic products
Specimens, intended purpose and analytical and clinical performance for diagnostic devices and systems.
Questions for the evidence file
- Luminaire configuration
- Control-gear identification
- Mounting conditions
- Optical measurement context
- Intended purpose
- Classification rationale
Record the exact edition and associated amendments, the assessed object, the evidence examined and the limits of the conclusion. Explore IESQ research for detailed product and standard studies.
Legal citation
No Commission citation record has been linked to this reference in the IESQ index. That is an index result, not a conclusion that the standard is uncited. Consult the relevant Commission list and Official Journal acts.
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