Russian standards PDF

In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 1. Terms, definitions and general requirements

Document status: Replaced by GOST R ISO 18113-1-2024

In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 2. In vitro diagnostic reagents for professional use

Document status: Replaced by GOST R ISO 18113-2-2024

In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 3. In vitro diagnostic instruments for professional use

Document status: Replaced by GOST R ISO 18113-3-2024

In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 5. In vitro diagnostic instruments for self-testing

Document status: Replaced by GOST R ISO 18113-5-2024

High efficiency air filters (EPA, HEPA and ULPA). Part 2. Aerosol production, measuring equipment, particle counting statistics

Document status: Replaced by GOST R ISO 29463-2-2024

High efficiency air filters (EPA, НЕРА and ULPA). Part 4. Determining leakage of filter elements (scan method)

Document status: Replaced by GOST R ISO 29463-4-2024