Belarus standards 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
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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
Geometrical product specifications (GPS). Partition. Vocabulary and basic concepts. Original standard UNE-EN ISO 18183-1-2024 in PDF full version. Additional info + preview on request
Document status: Active