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)
- SAE J1699/3-2012 Vehicle OBD II Compliance Test Cases
- SAE J1699/3-2009 Vehicle OBD II Compliance Test Cases
- SAE ARP5366-2017 Autopilot, Flight Director, and Autothrust Systems
VDI - Verein Deutscher Ingenieure
- VDI/VDE 2650 Blatt 7-2005 Requirements regarding self-monitoring and diagnosis in field instrumentation - Valves
- VDI/VDE 2650 Blatt 3-2004 Requirements regarding self-monitoring and diagnosis in field instrumentation - Flow measurement
- VDI/VDE 2650 Blatt 4-2004 Requirements regarding self-monitoring and diagnosis in field instrumentation - Level measurement
- VDI/VDE 2650 Blatt 5-2005 Requirements regarding self-monitoring and diagnosis in field instumentation - Temperature measurement
- VDI/VDE 2650 Blatt 6-2005 Requirements regarding self-monitoring and diagnosis in field instrumentation - Pressure measurement
- VDI/VDE 2650 Blatt 1-2004 Requirements regarding self-monitoring and diagnosis in field instrumentation - General requirements
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
- SAE R-264-2001 Engine Combustion Instrumentation and Diagnostics
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
- KS R ISO 16844-6-2017 Road vehicles — Tachograph systems — Part 6: Diagnostics
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
- SIS SS-ISO 4092:1991 Road vehicles — Diagnostic systems for motor vehicles — Vocabulary
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
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