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UV requirements for samples
UV requirements for samples, Total:44 items.
In the international standard classification, UV requirements for samples involves: Water quality, Domestic electrical appliances in general, Body care equipment, Domestic safety, Testing of metals, Laboratory medicine, Environmental testing, Mechanical testing, Manufacturing forming processes, Medical equipment.
German Institute for Standardization, UV requirements for samples
- DIN 19294-1:2020-08 Devices for the disinfection of water using ultraviolet radiation - Part 1: Devices equipped with UV low pressure lamps - Requirements and testing / Note: This standard is part of the DVGW body of rules.
- DIN 19294-1:2020 Devices for the disinfection of water using ultraviolet radiation - Part 1: Devices equipped with UV low pressure lamps - Requirements and testing
- DIN 19294-3:2020-08 Devices for the disinfection of water using ultraviolet radiation - Part 3: Reference radiometers for devices equipped with UV low pressure lamps - Requirements and testing / Note: This standard is part of the DVGW body of rules.
- DIN 19294-3:2020 Devices for the disinfection of water using ultraviolet radiation - Part 3: Reference radiometers for devices equipped with UV low pressure lamps - Requirements and testing
- DIN EN ISO 15193:2009-10 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO 15193:2009); German version EN ISO 15193:2009
- DIN EN ISO 15194:2009-10 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO 15194:2009); German version EN ISO 15194:2009
- DIN EN ISO 17511:2021-11 In vitro diagnostic medical devices - Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples (ISO 17511:2020); German version EN ISO 17511:2021
- DIN EN ISO 15193:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO 15193:2009); English version of DIN EN ISO 15193:2009-10
AT-ON, UV requirements for samples
- ONORM M 5873-1-2001 Plants for the disinfection of water using ultraviolet radiation - Requirements and testing - Low pressure mercury lamp plants
YU-JUS, UV requirements for samples
Professional Standard - Aviation, UV requirements for samples
- HB 5618.5-1988 Basic Product Drawing Management System (Lifesaving Specialty) Requirements for Product Drawings and Technical Documents
- HB 5613.4-1988 Basic product drawing management system (air-to-air missile major) Requirements for the preparation of design drawings and technical documents
Standard Association of Australia （SAA）, UV requirements for samples
- AS/NZS 60335.2.27:2004 Household and similar electrical appliances - Safety - Particular requirements for appliances for skin exposure to ultraviolet and infrared radiation
ZA-SANS, UV requirements for samples
- SANS 60335-2-27:2007 Household and similar electrical appliances - Safety Part 2-27: Particular requirements for appliances for skin exposure to ultraviolet and infrared radiation
未注明发布机构, UV requirements for samples
- BS EN ISO 15194:2009(2016) In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentation
- BS EN ISO 15193:2009(2016) In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for content and presentation of reference measurement procedures
Professional Standard - Agriculture, UV requirements for samples
- CNAS-EL-19：2021 Specific requirements for raw materials to be pure substances in the certification of reference material/standard sample producers
- CNAS-EL-19:2021 Specific requirements for raw materials to be pure substances in the certification of reference material/standard sample producers
International Organization for Standardization (ISO), UV requirements for samples
- ISO 17511:2020 In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
- ISO 21151:2020 In vitro diagnostic medical devices — Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samples
British Standards Institution (BSI), UV requirements for samples
- 19/30378312 DC BS ISO 21151. In vitro diagnostic medical devices. Measurement of quantities in samples of biological origin. Requirements for international harmonization protocols establishing metrological traceability of values assigned to calibrators and human samples
- BS EN ISO 15193:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures
- BS ISO 21151:2020 In vitro diagnostic medical devices. Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samples
- BS EN ISO 15194:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation
- BS 6920-2.3:2000 Suitability of non-metallic products for use in contact with water intended for human consumption with regard to their effect on the quality of the water - Methods of test - Appearance of water
- 19/30378309 DC BS EN ISO 17511. In vitro diagnostic medical devices. Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
- BS EN ISO 17511:2021 Tracked Changes. In vitro diagnostic medical devices. Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
RU-GOST R, UV requirements for samples
- GOST R 55046-2012 Technical diagnostics. Evaluation of residual resource of long used steel pipelines on the basis of samples mechanical tests results. General requirements
- GOST 30631-1999 General requirements for machines, instruments and other industrial products as to environment mechanical stability
US-CFR-file, UV requirements for samples
- CFR 15-758.5-2013 Commerce and foreign trade. Part758:Export clearance requirements. Section758.5:Conformity of documents and unloading of items.
国家市场监督管理总局、中国国家标准化管理委员会, UV requirements for samples
- GB/T 19702-2021 In vitro diagnostic medical devices—Measurement of quantities in samples of biological origin—Requirements for content and presentation of reference measurement procedures
- GB/T 19703-2020 In vitro diagnostic medical devices—Measurement of quantities in samples of biological origin—Requirements for certified reference materials and the content of supporting documentation
European Committee for Standardization (CEN), UV requirements for samples
- EN ISO 15193:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO 15193:2009)
Association Francaise de Normalisation, UV requirements for samples
- NF S92-019*NF EN ISO 15193:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures
- NF EN ISO 15193:2009 Dispositifs médicaux de diagnostic in vitro - Mesurage des grandeurs dans des échantillons d'origine biologique - Exigences relatives au contenu et à la présentation des procédures de mesure de référence
- NF S92-080:2020 In vitro diagnostic medical devices - Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samples
- NF EN ISO 15194:2009 Dispositifs médicaux de diagnostic in vitro - Mesurage des grandeurs dans les échantillons d'origine biologique - Exigences relatives aux matériaux de référence certifiés et au contenu de la documentation associée
ES-UNE, UV requirements for samples
- UNE-EN ISO 17511:2022 In vitro diagnostic medical devices - Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples (ISO 17511:2020)
Danish Standards Foundation, UV requirements for samples
- DS/ISO 17511:2021 In vitro diagnostic medical devices – Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
Korean Agency for Technology and Standards (KATS), UV requirements for samples
- KS P ISO 17511:2021 In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
KR-KS, UV requirements for samples
- KS P ISO 17511-2021 In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
AENOR, UV requirements for samples
- UNE-EN ISO 15193:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO 15193:2009)
- UNE-EN ISO 15194:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO 15194:2009)
Underwriters Laboratories (UL), UV requirements for samples
- UL 817 CRD-2016 UL Standard for Safety Cord Sets and Power-Supply Cords - Section Section / Paragraph Reference: Revise Par. 10.1.1.6 Subject: Adding requirements for an outdoor power supply cord employing SPT-2W and SPT-2RW cord for use in products covered by the Standa