Reference details
- Reference
- EN ISO 21535:2024
- Official title
- Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants (ISO 21535:2023)
- Organisation
- CEN
- 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
- Construction products and structural materials
Declared product performance, assessment methods and the relation between a product and its intended use in works.
- Medical devices
Intended medical purpose, device classification and the evidence associated with design, performance and lifecycle controls.
Questions for the evidence file
- Product-type identification
- Performance assessment
- Factory production control
- Declaration and installation scope
- 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.
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 (Regulation 2017/745)
Source: Generated on 17.6.2026
- Start date in source
- 2026-01-30
- Official Journal reference
- OJ L
An absent date or restriction field is not confirmation of current legal status.