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GOST R 54882-2011

Guidelines for regulatory auditing of quality management systems of medical device manufacturers. Part 2. Regulatory auditing strategy

Document status: Active

GOST 18301-72

Drinking water. Methods of determination of ozone residual content

Document status: Active

GOST R ISO 11222-2006

Air quality. Determination of the uncertainty of the time average of air quality measurements

Document status: Active

GOST 12.2.016-81

Occupational safety standards system. Gas compressing equipment. General safety requirements

Document status: Active

GOST 4.492-89

System of products quality indices. Biological veterinary preparations. Indices nomenclature

Document status: Active

GOST 12.2.140-2004

Small tractors. General requirements for safety

Document status: Active

GOST 31214-2016

Medical devices. Requirements for samples and documentation presented for toxicological tests, sanitary and chemical analyses, tests for sterility and pyrogenicity

Document status: Active

GOST R 50267.33-99

Medical electrical equipment. Part 2. Particular requirements for the safety of magnetic resonance equipment for medical diagnosis

Document status: Replaced by GOST R IEC 60601-2-33-2009

GOST R 51545-2000

Hydraulically operated portable emergency and rescue tools. Hydraulic power unit with motor drive. Basic parameters and dimensions. Safety requirements. Methods of testing and control

Document status: Active

GOST R ISO 28927-3-2012

Vibration. Evaluation of vibration emission of hand-held power tools. Part 3. Polishers and rotary, orbital and random orbital sanders

Document status: Active

GOST 31191.1-2004

Vibration and shock. Measurement and evaluation of human exposure to whole-body vibration. Part 1. General requirements

Document status: Active

GOST R 51959.2-2002

Non-invasive sphygmomanometers (measuring devices of arterial pressure). Part 2. Supplementary requirements for mechanical sphygmomanometers

Document status: Cancelled