STB PDF
In vitro diagnostic medical devices Information supplied by the manufacturer (labelling) Part 1- Terms, definitions, and general requirements (ISO 18113-1-2022). Original standard UNE-EN ISO 18113-1-2025 in PDF full version. Additional info + preview on request
Document status: Active
In vitro diagnostic medical devices Information supplied by the manufacturer (labelling) Part 2- In vitro diagnostic reagents for professional use (ISO 18113-2-2022). Original standard UNE-EN ISO 18113-2-2025 in PDF full version. Additional info + preview on request
Document status: Active
In vitro diagnostic medical devices Information supplied by the manufacturer (labelling) Part 3- In vitro diagnostic instruments for professional use (ISO 18113-3-2022). Original standard UNE-EN ISO 18113-3-2025 in PDF full version. Additional info + preview on request
Document status: Active
In vitro diagnostic medical devices Information supplied by the manufacturer (labelling) Part 4- In vitro diagnostic reagents for self-testing (ISO 18113-4-2022). Original standard UNE-EN ISO 18113-4-2025 in PDF full version. Additional info + preview on request
Document status: Active
In vitro diagnostic medical devices Information supplied by the manufacturer (labelling) Part 5- In vitro diagnostic instruments for self-testing (ISO 18113-5-2022). Original standard UNE-EN ISO 18113-5-2025 in PDF full version. Additional info + preview on request
Document status: Active
Plastics - Determination of the tendency of compounds and products based on vinyl chloride homopolymers and copolymers to evolve hydrogen chloride and any other acidic products at elevated temperatures - Part 3- Conductometric method (ISO 182-3-2023). Original standard UNE-EN ISO 182-3-2024 in PDF full version. Additional info + preview on request
Document status: Replaced by STB UNE-EN ISO 182-3-2026