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Biological evaluation of medical devices. Part 14. Identification and quantification of degradation products from ceramics
Document status: Active
Definition of acceptable level (degree) of risk and hazard industry-wide manufacturing equipment
Document status: Active
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
Drinking water. General requirements for organization and quality control methods
Document status: Active
Enclosing building structures crossing junction points by using pipe, which is made of polymeric materials. Fire resistance test
Document status: Active
Occupational safety standards system. Positive-displacement hydraulic drives and lubricating systems. General safety requirements
Document status: Withdrawn