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Instrument automatic diagnosis system

Instrument automatic diagnosis system, Total:134 items.

The international standard classification for "Instrument automatic diagnosis system" includes: Laboratory medicine , Industrial automation systems .

The Chinese standard classification for "Instrument automatic diagnosis system" includes: Medical laboratory equipment , Industrial automation and control device in general .


Group Standards of the People's Republic of China

  • T/CASME 451-2023 Technical requirements for instrumentation automation measurement and control equipment and systems
  • T/SHDSGY 059-2023 Automatic diagnostic ECG embedded software

General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China

  • GB/T 19634-2005 In vitro diagnostic test systems - General technical requirements for blood-glucose monitoring systems for self-testing
  • GB/T 41571-2022 The diagnosis method of energy efficiency in industry automation
  • GB/T 29791.5-2013 In vitro diagnostic medical devices―Information supplied by the manufacturer (labelling)―Part 5:In vitro diagnostic instruments for selftesting

未注明发布机构

  • DIN EN ISO 15197:2004 Test systems for in vitro diagnostics – requirements for blood glucose measuring systems for self-use in diabetes mellitus
  • DIN EN 591:2001 Instructions for use for in vitro diagnostic instruments for professional use
  • JEDEC JESD82-22.01-2023 INSTRUMENTATION CHIP DATA SHEET FOR FBDIMM DIAGNOSTIC SENSELINES

工业和信息化部/国家能源局

  • JB/T 12725-2016 Non-destructive testing instruments. Ultrasonic automatic detection system

国家市场监督管理总局、中国国家标准化管理委员会

  • GB/T 19634-2021 In vitro diagnostic test systems—General technical requirements for blood-glucose monitoring systems for self-testing

Military Standard of the People's Republic of China-General Armament Department

  • GJB 10102-2021 Diagnostic evaluation method of spacecraft control system

SCC

  • NS-EN 592:1994 In vitro diagnostic systems — Requirements for user manual for in vitro diagnostic instruments for home use
  • UNE-EN 592:2002 Instructions for use for in vitro diagnostic instruments for self-testing.
  • NS-EN 591:1994 In vitro diagnostic systems — Requirements for user manuals for in vitro diagnostic instruments for professional use
  • NS-EN 592:2002 Instructions for use for in vitro diagnostic instruments for self-testing
  • DANSK DS/EN 592:2002 Instructions for use for in vitro diagnostic instruments for self-testing
  • NS-EN 376:1992 In vitro diagnostic systems — Requirements for labelling of in vitro diagnostic reagents for self-testing
  • VDI/VDE 2650 BLATT 7-2006 Requirements for self-monitoring and diagnostics in field instrumentation — actuators
  • BS EN ISO 18113-5:2009 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic instruments for self-testing
  • 06/30146526 DC BS ISO 18113-5. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 5. In vitro diagnostic instruments for self-testing
  • DANSK DS/EN ISO 18113-5:2011 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing
  • AENOR UNE-EN 1658:1997 Marking requirements for in vitro diagnostic instruments.
  • VDI/VDE 2650 BLATT 7-2006 Requirements for self-monitoring and diagnostics in field instrumentation — actuators
  • NS-EN ISO 18113-5:2024 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2022)
  • DANSK DS/ISO 16844-6:2015 Road vehicles – Tachograph systems – Part 6: Diagnostics
  • UNE 26413-1:1991 ROAD VEHICLES. DIAGNOSTIC SYSTEMS FOR MOTOR VEHICLES. VOCABULARY.
  • AENOR UNE-EN ISO 18113-5:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
  • NS-EN ISO 18113-5:2011 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
  • NS-EN ISO 18113-5:2009 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
  • UNE-EN ISO 18113-5:2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
  • DANSK DS/EN 591:2001 Instructions for use for in vitro diagnostic instruments for professional use
  • NS-EN 591:2001 Instructions for use for in vitro diagnostic instruments for professional use
  • DIN EN ISO 18113-5 E:2007 Draft Document - Clinical laboratory testing and in vitro diagnostic medical systems - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/DIS 18113-5:2006); German version prEN ISO 18113...
  • VDI/VDE 2650 BLATT 4-2006 Requirements for self-monitoring and diagnostics in field instrumentation — level measurement
  • VDI/VDE 2650 BLATT 4-2006 Requirements for self-monitoring and diagnostics in field instrumentation — level measurement
  • VDI/VDE 2650 BLATT 6-2006 Requirements for self-monitoring and diagnostics in field instrumentation — pressure measurement
  • BS EN 592:1995 Specification for user manuals for in vitro diagnostic instruments for home use
  • VDI/VDE 2650 BLATT 5-2006 Requirements for self-monitoring and diagnostics in field instrumentation — temperature measurement
  • VDI/VDE 2650 BLATT 1-2006 Requirements for self-monitoring and diagnostics in field instrumentation — General requirements
  • DANSK DS/ISO 18434-2:2019 Condition monitoring and diagnostics of machine systems – Thermography – Part 2: Image interpretation and diagnostics
  • VDI/VDE 2650 BLATT 5-2006 Requirements for self-monitoring and diagnostics in field instrumentation — temperature measurement
  • VDI/VDE 2650 BLATT 6-2006 Requirements for self-monitoring and diagnostics in field instrumentation — pressure measurement
  • VDI/VDE 2650 BLATT 3-2006 Requirements for self-monitoring and diagnostics in field instrumentation — flow measurement
  • VDI/VDE 2650 BLATT 3-2006 Requirements for self-monitoring and diagnostics in field instrumentation — flow measurement
  • NS-EN 375:1992 In vitro diagnostic systems — Requirements for labelling of in vitro diagnostic reagents for professional use
  • BS EN 591:1995 Specification for user manuals for in vitro diagnostic instruments for professional use
  • UNE-EN 591:2001 Instructions for use for in vitro diagnostic instruments for professional use.

BE-NBN

  • NBN EN 592-1995 In vitro diagnostic systems - Requirements for user manual for in vitro diagnostic instruments for home use
  • NBN EN 591-1995 In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional use
  • NBN-EN 376-1992 In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testing

Association Francaise de Normalisation

  • NF S92-017:1995 IN VITRO DIAGNOSTIC SYSTEMS. REQUIREMENTS FOR USER MANUALS FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR HOME USE. (EUROPEAN STANDARD EN 592).
  • NF S92-016:1995 IN VITRO DIAGNOSTIC SYSTEMS. REQUIRMENTS FOR USER MANUELS FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR PROFESSIONAL USE. (EUROPEAN STANDARD EN 591).
  • NF S92-010-5:2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5 : in vitro diagnostic instruments for self-testing.
  • NF S92-010-5*NF EN ISO 18113-5:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5 : in vitro diagnostic instruments for self-testing
  • NF S92-011:1992 IN VITRO DIAGNOSTIC SYSTEMS. REQUIREMENTS FOR LABELLING OF IN VITRO DIAGNOSTIC REAGENTS FOR SELF-TESTING. (EUROPEAN STANDARD EN 376).
  • NF EN ISO 18113-5:2012 In vitro diagnostic medical devices - Information provided by the manufacturer (labelling) - Part 5: in vitro diagnostic instruments for self-testing
  • NF S92-018:1997 Requirements for marking of in vitro diagnostic instruments.
  • NF C74-336:1988 Medical electrical equipment. Ultrasound equipment for diagnostic. Classification of specified diagnostic applications.
  • NF ISO 18434-2:2019 Condition monitoring and diagnosis of machine systems - Thermography - Part 2: Image interpretation and diagnosis
  • NF ISO 13373-3:2015 Surveillance et diagnostic d'état des machines - Surveillance des vibrations - Partie 3 : lignes directrices pour le diagnostic des vibrations
  • NF EN ISO 15197:2015 In vitro diagnostic test systems - Requirements for self-monitoring blood glucose systems for the management of diabetes mellitus

European Committee for Standardization (CEN)

  • prEN 592-1991 In-vitro diagnostic systems; requirements for user manual of in-vitro diagnostic instruments for home use
  • prEN 591-1991 In-vitro diagnostic systems; requirements for user manual of in-vitro diagnostic instruments for professional use
  • EN ISO 18113-5:2011 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
  • EN 376:1992 In vitro diagnostic systems; requirements for labelling of in vitro diagnostic reagents for self-testing
  • EN 1658:1996 Requirements for Marking of in Vitro Diagnostic Instruments
  • EN ISO 18113-5:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing [Superseded: CEN EN 592]
  • prEN ISO 18113-5:2021 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/DIS 18113-5:2021)
  • FprEN ISO 18113-5 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/FDIS 18113-5:2022)
  • EN 592:2002 Instructions for Use in Vitro Diagnostic Instruments for Self-Testing
  • EN 592:1994 In Vitro Diagnostic Systems - Requirements for User Manuals for In Vitro Diagnostic Instruments for Home Use

Danish Standards Foundation

  • DS/EN 592:1995 In vitro diagnostic systems - Requirements for ser manuals for in vitro diagnostic instruments or home use
  • DS/EN 591:1995 In vitro diagnostic systems - Requirements for ser manuals for in vitro diagnostic instruments or professional use
  • DS/EN 376:1993 In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testing

GOSTR

  • GOST R EN 592-2010 Instructions for use for in vitro diagnostic instruments for self-testing

British Standards Institution (BSI)

  • BS EN ISO 18113-5:2024 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) - In vitro diagnostic instruments for self-testing
  • BS EN ISO 18113-5:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for self-testing
  • BS EN 592:2002 Instructions for use for in vitro diagnostic instruments for self-testing
  • BS ISO 16844-6:2022 Road vehicles. Tachograph systems. Diagnostic communication interfaces
  • BS ISO 18434-2:2019 Condition monitoring and diagnostics of machine systems. Thermography - Image interpretation and diagnostics
  • BS AU 206-2:1986 Diagnostic systems for road vehicles - Specification for graphical symbols for diagnostic testers
  • BS EN 1658:1997 Requirements for marking of in vitro diagnostic instruments
  • BS EN ISO 18113-3:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for professional use
  • BS ISO 13373-3:2015 Condition monitoring and diagnostics of machines. Vibration condition monitoring. Guidelines for vibration diagnosis
  • BS EN 591:2001 Instructions for use for in vitro diagnostic instruments for professional use
  • BS EN ISO 18113-3:2024 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) - In vitro diagnostic instruments for professional use
  • 21/30416045 DC BS EN ISO 18113-5. In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) - Part 5. In vitro diagnostic instruments for self-testing
  • BS ISO 13373-9:2017 Condition monitoring and diagnostics of machines. Vibration condition monitoring. Diagnostic techniques for electric motors

AT-ON

  • ONORM EN 376-1993 In vitro diagnostic Systems - Requirements for labelling of in vitro diagnostic reagents for serf-testing
  • ONORM EN 375-1993 In vitro diagnostic Systems - Requirements for labelling of in vitro diagnostic reagents for professional use

Japanese Industrial Standards Committee (JISC)

  • JIS D 5404:2000 Road vehicles -- Diagnostic systems -- Physical layer and diagnostic connector
  • JIS D 5404:2006 Road vehicles -- Diagnostic systems -- Physical layer and diagnostic connector

Society of Automotive Engineers (SAE)

VDI - Verein Deutscher Ingenieure

RU-GOST R

  • GOST 23434-1979 Technical diagnosis. Diagnosis means. Carburator engine ignition system. General technical requirements
  • GOST R ISO 18113-5-2015 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 5. In vitro diagnostic instruments for self-testing
  • GOST 17562-1972 Measuring instruments for functional diagnostic. Terms and definitions
  • GOST R ISO 18434-2-2021 Condition monitoring and diagnostics of machine systems. Thermography. Part 2. Image interpretation and diagnostics
  • GOST R 55991.1-2014 In vitro diagnostics medical devices. Part 1. Automatic analyzers for biochemical assays. Technical requirements for public procurement
  • GOST R 52122-2003 Technical diagnostics. Mainline locomotives. On-board diagnostic systems. General requirements
  • GOST R 55991.2-2014 In vitro diagnostics medical devices. Part 2. Automatic analyzer for immunoassays. Technical requirements for public procurement
  • GOST R 55991.4-2014 In vitro diagnostics medical devices. Part 4. Automatic analyzers for coagulation tests. Technical requirements for public procurement

Korean Agency for Technology and Standards (KATS)

  • KS P ISO 18113-5-2020 In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 5: In vitro diagnostic instruments for self-testing
  • KS C 1216-2001(2011) Manual scanning B-mode ultrasonic diagnostic equipment
  • KS R ISO 16844-6-2022 Road vehicles — Tachograph systems — Part 6: Diagnostics
  • KS R 0110-2001 Road vehicles-Diagnostic systems for motor vehicles-Vocabulary
  • KS P ISO 18113-5-2015(2020) In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 5: In vitro diagnostic instruments for self-testing
  • KS R 0110-2006 Road vehicles-Diagnostic systems for motor vehicles-Vocabulary

International Organization for Standardization (ISO)

  • ISO 18113-5:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing
  • ISO 18113-5:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing
  • ISO 14229:1998 Road vehicles - Diagnostic systems - Diagnostic services specification
  • ISO 18434-2:2019 Condition monitoring and diagnostics of machine systems — Thermography — Part 2: Image interpretation and diagnostics

SAE - SAE International

GSO

  • OS GSO ISO 18113-5:2016 In vitro diagnostic medical devices -- Information supplied by the manufacturer (labelling) -- Part 5: In vitro diagnostic instruments for self-testing
  • GSO ISO 18113-5:2016 In vitro diagnostic medical devices -- Information supplied by the manufacturer (labelling) -- Part 5: In vitro diagnostic instruments for self-testing
  • BH GSO ISO 18113-5:2017 In vitro diagnostic medical devices -- Information supplied by the manufacturer (labelling) -- Part 5: In vitro diagnostic instruments for self-testing
  • BH GSO ISO 16844-6:2017 Road Vehicles – Tachograph Systems – Part 6 : Diagnostics
  • OS GSO ISO 16844-6:2016 Road Vehicles – Tachograph Systems – Part 6 : Diagnostics
  • GSO ISO 16844-6:2016 Road Vehicles – Tachograph Systems – Part 6 : Diagnostics

KR-KS

GOST

  • GOST R 70937-2023 Intelligent systems for automatic monitoring and diagnostics of freight cars. General technical requirements

AENOR

  • UNE-EN ISO 18113-5:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)

ES-AENOR

  • UNE 23-507-1989 Fixed system for water spray. Automatic detection equipment

ASHRAE - American Society of Heating@ Refrigerating and Air-Conditioning Engineers@ Inc.

  • ASHRAE CH-99-5-2-1999 Automated Fault Detection and Diagnostics for Outdoor-Air Ventilation Systems and Economizers: Methodology and Results from Field Testing

SE-SIS

RO-ASRO

  • SR ISO 4092:1995 Road vehiclis - Diagnostic systems for motor vehicles Vocabulary

IN-BIS

  • IS 10269-1982 Specification for clinical and diagnostic instruments with hemocytometers