Guidelines for combining different single-mode fibre sub-categories
IEC TR 62000:2021 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy way to compare all the changes between the official IEC Standard and its previous edition.
IEC TR 62000:2021 provides guidelines concerning single-mode fibre inter-compatibility. A given category of single-…
Guidelines for combining different single-mode fibre sub-categories
IEC TR 62000:2021 provides guidelines concerning single-mode fibre inter-compatibility. A given category of single-mode fibre, for example B-655, can have different implementations by suitably optimising several of the following parameters: mode field diameter (hence effective area), chromatic dispersion coefficient, slope of the chromatic dispersion curve, cable cut-off wavelength. These…
Medical electrical equipment - Part 2-41: Particular requirements for the basic safety and essential...
IEC 60601-2-41:2021 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of SURGICAL LUMINAIRES and LUMINAIRES FOR DIAGNOSIS, hereafter referred to as ME EQUIPMENT.
If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies…
Digital audio interface - Part 3: Consumer applications
IEC 60958-3:2021 is available as IEC 60958-3:2021 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.IEC 60958-3:2021 specifies the consumer application of the interface for the inter-connection of digital audio equipment defined in IEC 60958-1. IEC 60958-3:2021 cancels and replaces the third edition…
Digital audio interface - Part 3: Consumer applications
IEC 60958-3:2021 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy way to compare all the changes between the official IEC Standard and its previous edition.
IEC 60958-3:2021 specifies the consumer application of the interface for the inter-connection of digital audio…
Digital audio interface - Part 3: Consumer applications
IEC 60958-3:2021 specifies the consumer application of the interface for the inter-connection of digital audio equipment defined in IEC 60958-1. IEC 60958-3:2021 cancels and replaces the third edition published in 2006, Amendment 1:2009 and Amendment 2:2015. This edition constitutes a technical revision. This edition includes the following significant technical changes with respect to the…
Lamp controlgear — Part 2-13: Particular requirements for d.c. or a.c. supplied electronic controlge...
1 Scope
This Standard specifies particular safety requirements for electronic controlgear for use on d.c. supplies
up to 380 V and a.c. supplies up to 600 V at 50 Hz or 60 Hz and at an output frequency that can deviate
from the supply frequency, associated with LED modules.
Notes:
1) A lamp controlgear for LED modules may also be referred to as “LED controlgear”, “LED driver”, “LED power…
CSA C22.2 No. 62031:21 LED modules for general lighting — Safety specifications -- CSA C22.2 nº 6203...
1 Scope
1.1
This Standard specifies general and safety requirements for
a) non-integrated light-emitting diode (LED) modules (LEDni modules) and semi-integrated LED
modules (LEDsi modules) for operation under constant voltage, constant current, or constant
power; and
b) integrated LED modules (LEDi modules) for use on dc supplies up to 250 V or ac supplies up to
600 V.
LED modules within…
Medical electrical equipment — Part 2-90: Particular requirements for basic safety and essential per...
This document applies to the basic safety and essential performance of respiratory high-flow therapy equipment, as defined in 201.3.220, hereafter also referred to as ME equipment or ME system, in combination with its accessories:
— intended for use with patients who can breathe spontaneously; and
— intended for patients who would benefit from improved alveolar gas exchange; and who would…
Medical electrical equipment - Part 2-90: Particular requirements for basic safety and essential per...
This document applies to the basic safety and essential performance of respiratory high-flow therapy equipment, as defined in 201.3.220, hereafter also referred to as ME equipment or ME system, in combination with its accessories:
- intended for use with patients who can breathe spontaneously; and
- intended for patients who would benefit from improved alveolar gas exchange; and who would…