| ASTM |
D5248 |
Standard Specification for Reclaimed 1,1,2-Trichloro 1,2,2-Trifluoroethane |
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| ASTM |
D4995 |
Standard Specifications for Electronic and Degreasing Grades of 1,1,2-Trichloro 1,2,2,-Trifluoroethane Solvent |
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| BSI |
BS R 1 |
Sizes and Forms of Civil Aircraft Radio Equipment |
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| BSI |
BS R 2 |
Basic Characteristics of Radio Service Selection and Intercommunication Systems for CI |
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| ASTM |
D6064 |
Standard Specification for HFC-227ea, 1,1,1,2,3,3,3-Heptafluoropropane (CF<inf>3</inf >CHFCF<inf>3</inf>) |
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| IEC |
IEC 60502-1 |
Power cables with extruded insulation and their accessories for rated voltages from 1 kV (Um = 1,2 kV) up to 30 kV (Um = 36 kV) - Part 1: Cables for rated voltages of 1 kV (Um = 1,2 kV) and 3 kV (Um = 3,6 kV) |
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| IEC |
IEC 61178-2-1 |
Quartz crystal units - A specification in the IEC Quality Assessment System for Electronic Components (IECQ) - Part 2: Sectional specification - Capability approval - Section 1: Blank detail specification |
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| IEC |
IEC 61261-2-1 |
Piezoelectric ceramic filters for use in electronic equipment - A specification in the IEC quality assessment system for electronic components (IECQ) - Part 2: Sectional specification - Qualification approval - Section 1: Blank detail specification - Assessment level E |
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| IEC |
IEC 61253-2-1 |
Piezoelectric ceramic resonators - A specification in the IEC quality assessment system for electronic components (IECQ) - Part 2: Sectional specification - Qualification approval - Section 1: Blank detail specification - Assessment level E |
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| CSA |
C22.2 NO. 60601-1-8 |
Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems (Adopted IEC 60601-1-8:2006, edition 2:2006 consolidated with amendment 1:2012 and amendment 2:2020, with Canadian deviations) | Appareils électromédicaux - Partie 1-8 : Exigences générales pour la sécurité de base et les performances essentielles - Norme collatérale : Exigences générales, essais et guide pour les systèmes d’alarme des appareils et des systèmes électromédicaux (norme IEC 60601-1-8:2006 adoptée, édition 2:2006 consolidée par l’amendement 1:2012 et l’amendement 2:2020, avec exigences propres au Canada) |
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| CSA |
CAN/CSA-C22.2 NO. 60601-1-8:08 + A1:14 + A2:21 (R2023) (CONSOLIDATED) |
Medical electrical equipment — Part 1-8: General requirements for basic safety and essential performance — Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems (Adopted IEC 60601-1-8:2006, edition 2:2006 consolidated with amendment 1:2012 and amendment 2:2020, with Canadian deviations) | Appareils électromédicaux — Partie 1-8 : Exigences générales pour la sécurité de base et les performances essentielles — Norme collatérale : Exigences générales, essais et guide pour les systèmes d’alarme des appareils et des systèmes électromédicaux (norme IEC 60601-1-8:2006 adoptée, édition 2:2006 consolidée par l’amendement 1:2012 et l’amendement 2:2020, avec exigences propres au Canada) |
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| ISO |
ISO 500-1 |
Agricultural tractors - Rear-mounted power take-off types 1, 2, 3 and 4 - Part 1: General specifications, safety requirements, dimensions for master shield and clearance zone |
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| IEC |
IEC 61067-3-1 |
Glass and glass polyester fibre woven tapes - Part 3: Specifications for individual materials - Sheet 1: Type 1, 2 and 3 tapes |
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| ISO |
ISO/IEC 11160-1 |
Information technology - Office equipment - Minimum information to be included in specification sheets - Printers - Part 1: Class 1 and Class 2 printers |
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| CSA |
CSA C22.2 NO. 60601-1-3:09 + A1:15 + A2:22 (CONSOLIDATED) (R2024) |
Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral standard: Radiation protection in diagnostic X-ray equipment (Adopted IEC 60601-1:2008, edition 2:2008 consolidated with amendment 1:2013 and amendment 2:2021, with Canadian deviations) I| Appareils électromédicaux - Partie 1-3: Exigences générales pour la sécurité de base et les performances essentielles - Norme collatérale: Radioprotection dans les appareils à rayonnement X de diagnostic (norme IEC 60601-1:2008 adoptée, édition 2:2008 consolidée par l’amendement 1:2013 et l’amendement 2:2021, avec exigences propres au Canada) |
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| CSA |
C22.2 NO. 60601-1-3 |
Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral standard: Radiation protection in diagnostic X-ray equipment (Adopted IEC 60601-1:2008, edition 2:2008 consolidated with amendment 1:2013 and amendment 2:2021, with Canadian deviations) I| Appareils électromédicaux - Partie 1-3: Exigences générales pour la sécurité de base et les performances essentielles - Norme collatérale: Radioprotection dans les appareils à rayonnement X de diagnostic (norme IEC 60601-1:2008 adoptée, édition 2:2008 consolidée par l’amendement 1:2013 et l’amendement 2:2021, avec exigences propres au Canada) |
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| ASTM |
D6541 |
Standard Specification for HFC-236fa, 1,1,1,3,3,3–Hexafluoropropane, (CF<inf>3</inf >CH<inf>2</inf>CF<inf>3</inf>) |
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| ASTM |
D5316 |
Standard Test Method for 1,2-Dibromoethane and 1,2-Dibromo-3-Chloropropane in Water by Microextraction and Gas Chromatography |
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| CSA |
CSA E60335-2-61:11 (R2021) |
Household and similar electrical appliances - Safety - Part 2-61: Particular requirements for thermal storage room heaters (Adopted IEC 60335-2-61:2002 + A1:2005 + A2:2008, edition 2:2002 consolidated with amendment 1:2005 and amendment 2:2008, with Canadian deviations) | Appareils électrodomestiques et analogues - Sécurité- Partie 2-61 : Règles particulières pour les appareils de chauffage àaccumulation (norme IEC 60335-2-61:2002 + A1:2005 + A2:2008 adoptée, édition 2:2002 consolidée par l'amendement 1:2005 et l'amendement 2:2008, avec exigences propres au Canada) |
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| CSA |
C22.2 NO. 60529 |
Degrees of protection provided by enclosures (IP Code) (Adopted IEC 60529:1989, edition 2:1989 consolidated with amendment 1:1999 and amendment 2:2013, with Canadian deviations) | Degrés de protection procurés par les enveloppes (Code IP) (norme IEC 60529:1989 adoptée , édition 2:1989 consolidée par l’amendement 1:1999 et l’amendement 2:2013, avec exigences propres au Canada) |
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| CSA |
CSA C22.2 NO. 60529:16 (R2021) |
Degrees of protection provided by enclosures (IP Code) (Adopted IEC 60529:1989, edition 2:1989 consolidated with amendment 1:1999 and amendment 2:2013, with Canadian deviations) | Degrés de protection procurés par les enveloppes (Code IP) (norme IEC 60529:1989 adoptée , édition 2:1989 consolidée par l’amendement 1:1999 et l’amendement 2:2013, avec exigences propres au Canada) |
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| CSA |
CSA ISO/IEC 17839-2:16/A1:22 |
Amendment 1:2022 to CSA ISO/IEC 17839-2:16, Information technology — Biometric System-on-Card — Part 2: Physical characteristics - Amendment 1: Additional specifications for fingerprint biometric capture devices (Adopted amendment 1:2021 to ISO/IEC 17839-2:2015) |
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| CSA |
CAN/CSA-C22.2 NO. 60601-1-9:15 + A1:15 + A2:21 (CONSOLIDATED) (R2024) |
Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral standard: Requirements for environmentally conscious design (Adopted IEC 60601-1-9:2007, edition 1:2007 consolidated with amendment 1:2013 and amendment 2:2020, with Canadian deviations) | Appareils électromédicaux - Partie 1-9 : Exigences générales pour la sécurité de base et les performances essentielles - Norme collatérale: Exigences pour une conception écoresponsable (norme IEC 60601-1-9:2007 adoptée, édition 1:2007, consolidée par l'amendement 1:2013 et l'amendement 2:2020, avec exigences propres au Canada) |
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| CSA |
C22.2 NO. 60601-1-10 |
Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers (Adopted IEC 60601-1-10:2007, edition 1:2007 consolidated with amendment 1:2013 and amendment 2:2020, with Canadian deviations) | Appareils électromédicaux - Partie 1-10 : Exigences générales pour la sécurité de base et les performances essentielles - Norme collatérale : Exigences pour le développement des régulateurs physiologiques en boucle fermée (norme IEC 60601-1-10:2007 adoptée, édition 1:2007 consolidée par l’amendement 1:2013 et l’amendement 2:2020, avec exigences propres au Canada) |
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