Reference details
- Reference
- EN 80601-2-58:2009
- Official title
- Medical electrical equipment - Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery
- Organisation
- CENELEC
- Publisher status in source
- WithdrawnThis 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
- Medical devices
Intended medical purpose, device classification and the evidence associated with design, performance and lifecycle controls.
Questions for the evidence file
- Intended purpose
- Classification rationale
- Risk management
- Verification and performance evidence
- Clinical evidence scope
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.
Legislation reference records
The following records come from Commission information lists. A source listing, a publication status and a legal presumption of conformity answer different questions. Check the applicable Official Journal acts, dates and restrictions for the intended claim.
Medical devices (Directive 93/42/EEC)
An absent date or restriction field is not confirmation of current legal status.