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DSTU

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DSTU EN ISO 10893-11:2015

Non-destructive testing of steel pipes. Part 11. Automated ultrasonic inspection of the weld of welded steel pipes to detect longitudinal and

DSTU EN ISO 10893-12:2015

Non-destructive testing of steel pipes. Part 12. Automated ultrasonic thickness control around the entire circumference of seamless and welded steel pipes (except for pipes obtained by submerged arc welding)

DSTU EN ISO 10893-2:2015

Non-destructive testing of steel pipes. Part 2. Automated eddy current inspection of steel seamless and welded pipes (except for pipes made by submerged arc welding) to detect defects

DSTU EN ISO 10893-3:2015

Non-destructive testing of steel pipes. Part 3. Automated control by magnetic flux scattering around the entire circumference of seamless and welded ferromagnetic steel pipes to detect longitudinal and

DSTU EN ISO 10893-4:2015

Non-destructive testing of steel pipes. Part 4. Capillary inspection of seamless steel welded pipes to detect surface defects

DSTU EN ISO 10893-6:2015

Non-destructive testing of steel pipes. Part 6. Radiographic inspection of weld steel pipes for defect detection

DSTU EN ISO 10893-7:2015

Non-destructive testing of steel pipes. Part 7. Digital radiographic inspection of weld steel pipes for defect detection

DSTU EN ISO 10893-8:2015

Non-destructive testing of steel pipes. Part 8. Automated ultrasonic inspection of steel seamless and welded pipes to detect delamination defects

DSTU EN ISO 10893-9:2015

Non-destructive testing of steel pipes. Part 9. Automated ultrasonic inspection for the detection of strip / sheet bundle defects used in the manufacture of welded steel tubes

DSTU EN ISO 10931:2015

Systems of plastic pipelines for industrial use. Field of (vinylidene fluoride) (PVDF). Specifications for components and systems

DSTU EN ISO 10993-1:2015

Biological evaluation of medical devices. Part 1. Assessment and testing as part of the risk management process

DSTU EN ISO 10993-11:2015

Biological evaluation of medical devices. Part 11. Systemic toxicity test

DSTU EN ISO 10993-12:2015

Biological evaluation of medical devices. Part 12. Sampling and reference materials

DSTU EN ISO 10993-13:2015

Biological evaluation of medical devices. Part 13. Qualitative and quantitative analysis of degradation products of polymer medical devices

DSTU EN ISO 10993-14:2015

Biological evaluation of medical devices. Part 14. Identification and quantification of ceramic pre-products

DSTU EN ISO 10993-15:2015

Biological evaluation of medical devices. Part 15. Qualitative and quantitative analysis of degradation products of metals and alloys

DSTU EN ISO 10993-16:2015

Biological evaluation of medical devices. Part 16. Construction of toxicokinetic studies of degradation and leaching products

DSTU EN ISO 10993-17:2015

Biological evaluation of medical devices. Part 17. Establishment of acceptable limits for viluvovuvial substances

DSTU EN ISO 10993-18:2015

Biological evaluation of medical devices. Part 18. Determination of chemical properties

DSTU EN ISO 10993-3:2015

Biological evaluation of medical devices. Part 3. Test for genotoxicity, carcinogenicity and reproductive toxicity

DSTU EN ISO 10993-4:2015

Biological evaluation of medical devices. Part 4. Selection of tests that interact with blood

DSTU EN ISO 10993-5:2015

Biological evaluation of medical devices. Part 5. In vitro cytotoxicity test

DSTU EN ISO 10993-6:2015

Biological evaluation of medical devices. Part 6. Tests for local effects after implantation

DSTU EN ISO 10993-7:2015

Biological evaluation of medical devices. Part 7. Residues after ethylene oxide sterilization

DSTU EN ISO 10993-9:2015

Biological evaluation of medical devices. Part 9. Principles of qualitative and quantitative analysis of potential degradation products

DSTU EN ISO 11105:2015

Small vessels. Engine room ventilation and

DSTU EN ISO 11135-1:2015

Sterilization of medical devices with ethylene oxide. Part 1. Requirements for the development, validation and ongoing monitoring of the sterilization process for medical devices

DSTU EN ISO 11137-1:2015

Sterilization of medical devices. Radiation sterilization. Part 1. Requirements for the development, validation and ongoing monitoring of the sterilization process for medical devices

DSTU EN ISO 11137-2:2015

Sterilization of medical devices. Radiation sterilization. Part 2. Establishment of a sterilization dose

DSTU EN ISO 11138-2:2015

Sterilization of medical products. Biological indicators. Part 2. Biological indicators for sterilization with ethylene oxide

DSTU EN ISO 11138-3:2015

Sterilization of medical products. Biological indicators. Part 3. Biological indicators for wet heat sterilization

DSTU EN ISO 11140-1:2015

Sterilization of medical devices. Chemical indicators. Part 1. General requirements

DSTU EN ISO 11140-3:2015

Sterilization of medical devices. Chemical indicators. Part 3. Second-class indicator systems for testing with a Bowie and Dick type test for steam penetration

DSTU EN ISO 11192:2015

Small vessels. Graphic Conventions

DSTU EN ISO 11197:2015

Medical power supplies. Individual requirements

DSTU EN ISO 11200:2015

Acoustics. The noise generated by machinery and equipment. Recommendations on the use of basic standards for determining sound pressure levels at the workplace and at other characteristic points

DSTU EN ISO 11203:2015

Acoustics. The noise generated by machinery and equipment. Determination of sound pressure levels at the workplace and at other characteristic points by sound power level

DSTU EN ISO 1135-4:2015

Medical devices for blood transfusion. Part 4. Disposable Blood Transfusion Kits

DSTU EN ISO 11547:2015

Small vessels. Trigger protection

DSTU EN ISO 11591:2015

Small vessels with an engine. Steering field of view

DSTU EN ISO 11592:2015

Small vessels with hull up to 8 m long. Determination of maximum engine power

DSTU EN ISO 11607-1:2015

Medical sterilized products. Packaging. Part 1. Basic requirements for materials, sterile barrier and packaging systems

DSTU EN ISO 11607-2:2015

Medical sterilized products. Packaging. Part 2. Validation requirements

DSTU EN ISO 11688-1:2015

Acoustics. Practical recommendations for the design of low-noise machines and equipment. Part 1. Planning

DSTU EN ISO 11737-1:2015

Sterilization of medical equipment. Microbiological methods. Part 1. Determination of the population of microorganisms on products

DSTU EN ISO 11737-2:2015

Sterilization of medical equipment. Microbiological methods. Part 2. Sterility tests performed to determine, validate and maintain the sterilization process.

DSTU EN ISO 11810-1:2015

Lasers and laser equipment. Test method and classification of surgical sheets and / or covers to protect patients from resistance to laser radiation. Part 1. Primary ignition and penetration

DSTU EN ISO 11810-2:2015

Lasers and laser equipment. Test method and classification of surgical sheets and / or covers to protect patients from resistance to laser radiation. Part 2. Secondary ignition

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