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CAN/CSA C22.2 NO. 60079-29-1:12 : Explosive atmospheres - Part 29-1: Gas detectors - Performance requirements of detectors for flammable gases (Adopted IEC 60079-29-1:2007, first edition, 2007-08, with Canadian deviations)

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Scope

This part of IEC 60079-29 specifies general requirements for construction, testing and performance, and describes the test methods that apply to portable, transportable and fixed apparatus for the detection and measurement of flammable gas or vapour concentrations with air. The apparatus, or parts thereof, are intended for use in potentially explosive atmospheres (see 3.1.8) and in mines susceptible to firedamp.

This standard is also applicable when an apparatus manufacturer makes any claims regarding any special features of construction or superior performance that exceed these minimum requirements. In these cases, all such claims should be verified and the test procedures should be extended or supplemented, where necessary, to verify the performance claimed by the manufacturer. When verifying the superior performance of one criterion, other performance criteria are not required to meet the standards minimum requirements, however, these reduced claimed performance criteria (as confirmed in the manufactures Installation Manual) should also be verified. (e.g. temperature range of 0 °C to 60 °C; 0 °C to 40 °C at ±10 % accuracy and 40 °C to 60 °C at ±15 % (manufacturers claimed accuracy). The additional tests should be agreed between the manufacturer and test laboratory and identified and described in the test report.

This standard is applicable to flammable gas detection apparatus intended to provide an indication, alarm or other output function; the purpose of which is to give a warning of a potential explosion hazard and in some cases, to initiate automatic or manual protective action(s).

This standard is applicable to apparatus, including the integral sampling systems of aspirated apparatus, intended to be used for commercial, industrial and non-residential safety applications.

This standard does not apply to external sampling systems, or to apparatus of laboratory or scientific type, or to apparatus used only for process control purposes. It also does not apply to open path (line of sight) area monitors. For apparatus used for sensing the presence of multiple gases, this standard applies only to the detection of flammable gas or vapour.

This standard supplements and modifies the general requirements of IEC 60079-0. Where a requirement of this standard conflicts with a requirement of IEC 60079-0, the requirement of IEC 60079-29-1 will take precedence.

NOTE 1 IEC 60079-29-1 is intended to provide for the supply of apparatus giving a level of safety and performance suitable for general purpose applications. However, for specific applications, a prospective purchaser (or an appropriate authority) may additionally require the apparatus to be submitted to particular tests or approval. For example, group I apparatus (i.e. apparatus to be used in mines susceptible to firedamp) may not be permitted to be used without the additional, prior approval of the relevant authority in mines under its jurisdiction. Such particular tests/approval are to be regarded as additional to and separate from the provisions of the standards referred to above and do not preclude certification to or compliance with these standards.

NOTE 2 All apparatus calibrated on specific gases or vapours can not be expected to correctly indicate on other gases or vapours.

NOTE 3 For the purposes of this standard, the terms "lower flammable limit (LFL)" and "lower explosive limit (LEL)" are deemed to be synonymous, and likewise the terms "upper flammable limit (UFL)" and "upper explosive limit (UEL)" are deemed to be synonymous. For ease of reference, the two abbreviations LFL and UFL may be used hereinafter to denote these two sets of terms. It should be recognized that particular authorities having jurisdiction may have overriding requirements that dictate the use of one of these sets of terms and not the other.

NOTE 4 For the purposes of this standard, the term -indicating up to a volume fraction of X %- includes apparatus with an upper limit of the measuring range equal to or less than X %.

CAN/CSA C22.2 No. 60079-7:12 : Explosive atmospheres - Part 7: Equipment protection by increased safety "e" (Adopted IEC 60079-7:2006, fourth edition, 2006-07, with Canadian deviations)

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Scope

The requirements of the IEC 60079 series of Standards cover protection techniques with respect to explosion hazard only. The CAN/CSA-C22.2 No. 60079 series of Standards (based on the adoption of corresponding IEC Standards) is to be used in conjunction with other applicable Standards containing the appropriate electrical safety requirements for general use equipment. General requirements for electrical products are as indicated in CSA C22.2 No. 0.

Group I electrical equipment intended for use in mines susceptible to firedamp is regulated by the provinces and territories of Canada. Such types of equipment (e.g., caplights) should be referred to the respective authority having jurisdiction.

CAN/CSA C22.2 No. 60079-2:12 : Explosive atmospheres - Part 2: Equipment protection by pressurized enclosure "p" (Adopted IEC 60079-2:2007, fifth edition, 2007-02, with Canadian deviations)

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Scope

This part of IEC 60079 contains the specific requirements for the construction and testing of electrical apparatus with pressurized enclosures, of type of protection "p", intended for use in explosive gas atmospheres. It specifies requirements for pressurized enclosures containing a limited release of a flammable substance.

This standard supplements and modifies the general requirements of IEC 60079-0. Where a requirement of this standard conflicts with a requirement of IEC 60079-0, the requirements of this standard takes precedence.

This standard does not contain the requirements for:


- pressurized enclosures where the containment system may release
a) air with an oxygen content greater than normal, or
b) oxygen in combination with inert gas in a proportion greater than 21 %;
- pressurized rooms or analyser houses; see IEC 60079-13 and IEC 60079-16.

NOTE 1 Due to the safety factors incorporated in the type of protection, the uncertainty of measurement inherent in good quality, regularly calibrated measurement equipment is considered to have no significant detrimental effect and need not be taken into account when making the measurements necessary to verify compliance of the equipment with the requirements of this standard.

NOTE 2 When the user acts in the role of the manufacturer, it is typically the user's responsibility to ensure that all relevant parts of this standard are applied to the manufacturing and testing of the equipment. NOTE 3 Types of protection "px" and "py"provide Equipment Protection Levels (EPL) Mb or Gb. Type of protection "pz" provides Equipment Protection Level (EPL) Gc. For further information, see Annex H.

CAN/CSA C22.2 NO. 80601-2-56:12 : Medical electrical equipment - Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement (Adopted ISO 80601-2-56:2009, first edition, 2009-10-01)

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Replacement:

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of a CLINICAL THERMOMETER in combination with its ACCESSORIES, hereafter referred to as ME EQUIPMENT. This standard specifies the general and technical requirements for electrical CLINICAL THERMOMETERS. This standard applies to all electrical CLINICAL THERMOMETERS that are used for measuring the body temperature of PATIENTS.

CLINICAL THERMOMETERS can be equipped with interfaces to accommodate secondary indicators, printing equipment, and other auxiliary equipment to create ME SYSTEMS. This standard does not apply to auxiliary equipment.

ME EQUIPMENT that measures a temperature not as a primary purpose, but as a secondary function, is outside the scope of this standard.

EXAMPLE 1 Swan-Ganz thermodilution determination of cardiac output is not in the scope of this standard.

EXAMPLE 2 A Foley catheter that includes a temperature PROBE is in the scope of this standard.

EXAMPLE 3 PATIENT heating ME EQUIPMENT that includes a skin temperature measurement such as infant incubators, heating blankets, heating pads and heating mattresses are not in the scope of this standard, unless they indicate a temperature of a REFERENCE BODY SITE in which they are in the scope of this standard.

Requirements for ME EQUIPMENT intended to be used for non-invasive human febrile temperature screening of groups of individuals under indoor environmental conditions are given in IEC 80601-2-59:2008 and such ME EQUIPMENT is not covered by this standard.

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 both to ME EQUIPMENT and to ME SYSTEMS, as relevant.

HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in IEC 60601-1:2005, 7.2.13 and 8.4.1.

NOTE Additional information can be found in IEC 60601-1:2005, 4.2.

CAN/CSA C22.2 NO. 80601-2-56:12 : Medical electrical equipment - Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement (Adopted ISO 80601-2-56:2009, first edition, 2009-10-01)

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Scope

Replacement:

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of a CLINICAL THERMOMETER in combination with its ACCESSORIES, hereafter referred to as ME EQUIPMENT. This standard specifies the general and technical requirements for electrical CLINICAL THERMOMETERS. This standard applies to all electrical CLINICAL THERMOMETERS that are used for measuring the body temperature of PATIENTS.

CLINICAL THERMOMETERS can be equipped with interfaces to accommodate secondary indicators, printing equipment, and other auxiliary equipment to create ME SYSTEMS. This standard does not apply to auxiliary equipment.

ME EQUIPMENT that measures a temperature not as a primary purpose, but as a secondary function, is outside the scope of this standard.

EXAMPLE 1 Swan-Ganz thermodilution determination of cardiac output is not in the scope of this standard.

EXAMPLE 2 A Foley catheter that includes a temperature PROBE is in the scope of this standard.

EXAMPLE 3 PATIENT heating ME EQUIPMENT that includes a skin temperature measurement such as infant incubators, heating blankets, heating pads and heating mattresses are not in the scope of this standard, unless they indicate a temperature of a REFERENCE BODY SITE in which they are in the scope of this standard.

Requirements for ME EQUIPMENT intended to be used for non-invasive human febrile temperature screening of groups of individuals under indoor environmental conditions are given in IEC 80601-2-59:2008 and such ME EQUIPMENT is not covered by this standard.

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 both to ME EQUIPMENT and to ME SYSTEMS, as relevant.

HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in IEC 60601-1:2005, 7.2.13 and 8.4.1.

NOTE Additional information can be found in IEC 60601-1:2005, 4.2.

CAN/CSA C22.2 NO. 80601-2-35:12 : Medical electrical equipment - Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads or mattresses and intended for heating in medical use (Adopted IEC 80601-2-35:2009, second edition, 2009-10, with Canadian deviations)

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Replacement:

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of HEATING DEVICES using BLANKETS, PADS or MATTRESSES in medical use, also referred to as ME EQUIPMENT. HEATING DEVICES intended to prewarm a bed are included in the scope of this International Standard.

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 both to ME EQUIPMENT and to ME SYSTEMS, as relevant.

If a clause or subclause is specifically intended to apply to a specifically defined type of ME EQUIPMENT, as is the case with FORCED AIR DEVICES, then the clause or subclause is entitled as such. Clauses or subclauses that apply to all types of ME EQUIPMENT within the scope of this standard are not specifically entitled.

HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the general standard.

NOTE See also 4.2 of the general standard.

This particular standard does not apply to:
- HEATING DEVICES intended for physiotherapy;
- radiant warmers; for information, see IEC 60601-2-21 [12]2;
- incubators; for information, see IEC 60601-2-19 [10];
- transport incubators, for information, see IEC 60601-2-20 [11];
- cooling devices.

CAN/CSA 14543-5-4-12 : Information technology - Home electronic system (HES) architecture - Part 5-4: Intelligent grouping and resource sharing for HES Class 2 and Class 3 - Device validation (Adopted ISO/IEC 14543-5-4:2010, first edition, 2011-11)

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Scope

Replacement:

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of HEATING DEVICES using BLANKETS, PADS or MATTRESSES in medical use, also referred to as ME EQUIPMENT. HEATING DEVICES intended to prewarm a bed are included in the scope of this International Standard.

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 both to ME EQUIPMENT and to ME SYSTEMS, as relevant.

If a clause or subclause is specifically intended to apply to a specifically defined type of ME EQUIPMENT, as is the case with FORCED AIR DEVICES, then the clause or subclause is entitled as such. Clauses or subclauses that apply to all types of ME EQUIPMENT within the scope of this standard are not specifically entitled.

HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the general standard.

NOTE See also 4.2 of the general standard.

This particular standard does not apply to:
- HEATING DEVICES intended for physiotherapy;
- radiant warmers; for information, see IEC 60601-2-21 [12]2;
- incubators; for information, see IEC 60601-2-19 [10];
- transport incubators, for information, see IEC 60601-2-20 [11];
- cooling devices.

CAN/CSA C22.2 No. 61241-4:12 : Electrical apparatus for use in the presence of combustible dust - Part 4: Type of protection "pD" (Adopted IEC 61241-4:2001, first edition, 2001-03, with Canadian deviations)

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1 Scope

This part of IEC 61241 gives requirements on the design, construction, testing and marking of electrical apparatus for use in combustible dust atmospheres in which a protective gas (air or inert gas), maintained at a pressure above that of the external atmosphere, is used to prevent the entry of dust which might otherwise lead to the formation of a combustible mixture within enclosures which do not contain a source of combustible dust.

This standard contains the specific requirements for construction and testing, including protective requirements that apply to electrical apparatus with type of protection pressurization "pD" intended for use in potentially combustible dust atmospheres.

This standard includes the requirements for the construction of the enclosure and its associated components, including, if any, the inlet and outlet ducts for the protective gas, and for the safety provisions and devices necessary to ensure that pressurization is established and maintained for type of protection pressurization "pD".

Requirements for pressurized enclosures with an internal source of dust release are not included in this standard.

This standard does not cover the requirements for pressurized rooms with or without internal sources of dust release.

This standard does not apply to dusts of explosives which do not require atmospheric oxygen for combustion or to pyrophoric substances.

This standard does not cover combined gas and dust hazard. Those requirements are under consideration.

The requirements contained in this standard are supplementary to those in IEC 61241-1-1.

CAN/CSA C22.2 No. 60079-31:12 : Electrical apparatus for use in the presence of combustible dust - Part 4: Type of protection "pD" (Adopted IEC 61241-4:2001, first edition, 2001-03, with Canadian deviations)

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This part of IEC 60079 is applicable to electrical equipment protected by enclosure and surface temperature limitation for use in explosive dust atmospheres. It specifies requirements for design, construction and testing of electrical equipment.

This standard supplements and modifies the general requirements of IEC 60079-0. Where a requirement of this standard conflicts with a requirement of IEC 60079-0, the requirement of this standard shall take precedence.

This standard does not apply to dusts of explosives, which do not require atmospheric oxygen for combustion, or to pyrophoric substances.

This standard does not apply to electrical equipment intended for use in underground parts of mines as well as those parts of surface installations of such mines endangered by firedamp and/or combustible dust.

This standard does not take account of any risk due to an emission of flammable or toxic gas from the dust.

NOTE 1 The application of electrical equipment in atmospheres, which may contain combustible dust as well as explosive gas, whether simultaneously or separately, may require additional protective measures.

NOTE 2 Where the equipment has to meet other environmental conditions, for example, protection against ingress of water and resistance to corrosion, additional methods of protection may be necessary. The method used should not adversely affect the integrity of the enclosure.

CAN/CSA C22.2 No. 60079-15:12 : Information technology - Home electronic system (HES) architecture - Part 5-4: Intelligent grouping and resource sharing for HES Class 2 and Class 3 - Device validation (Adopted ISO/IEC 14543-5-4:2010, first edition, 2011-11)

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This part of IEC 60079 specifies requirements for the construction, testing and marking for Group II electrical apparatus with type of protection, "n" intended for use in explosive gas atmospheres.

This part is applicable to non-sparking electrical apparatus and also to electrical apparatus with parts or circuits producing arcs or sparks or having hot surfaces which, if not protected in one of the ways specified in this standard, could be capable of igniting a surrounding explosive gas atmosphere. This standard describes several different methods by which this can be achieved which may be combined with other methods described in IEC 60079-0.

CSA B182.14-12/B182.15-12 : Profile steel reinforced polyethylene (SRPE) storm sewer pipe and fittings/Profile steel reinforced polyethylene (SRPE) sewer pipe and fittings

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This Standard specifies requirements for profile steel reinforced polyethylene (SRPE) sewer pipe and fittings for sanitary sewer and other gravity-flow applications.

Profile wall pipe in this standard includes open profile pipe of helical construction, with a smooth interior and sizes based on controlled inside diameter. The pipe can be perforated, for specific applications, as required.

Notes:
(1) Pipe and fittings manufactured in accordance with this Standard should be installed in accordance with CSA B182.11.
(2) The structural design of this product should be in accordance with the manufacturer's recommendations.
(3) Refer to Annex A for recommended quality control test frequencies.
(4) Refer to Annex B for base inside diameters used to determine installation deflection limits.
(5) Refer to Annex C for fitting patterns covered by this Standard.
(6) The ordering recommendations in Annex D should be followed to ensure that the requested products are described adequately.

CAN/CSA C22.2 NO. 60601-2-46:12 : Medical electrical equipment - Part 2-46: Particular requirements for the basic safety and essential performance of operating tables (Adopted IEC 60601-2-46:2010, second edition, 2010-12)

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Replacement:

This particular standard specifies safety requirements for OPERATING TABLES, whether or not having electrical parts, including TRANSPORTERS, used for the transportation of the table top to or from the base or pedestal of an OPERATING TABLE with detachable table top.

NOTE See also 4.2 of the General Standard.
This particular standard does not apply to
- dental patient chairs;
- examination chairs and couches;
- patient-supporting systems of diagnostic and therapeutic devices;
- OPERATING TABLE heating blankets;
- patient transfer equipment;
- delivery tables and beds;
- medical beds;
- field tables.

NOTE If OPERATING TABLES will be used in combination with diagnostic and/or therapeutic devices the relevant requirements of each particular standard have to be considered.

CAN/CSA C22.2 NO. 60601-2-33:12 : Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis

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CSA Preface

This is the second edition of CAN/CSA-C22.2 No. 60601-2-33, Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis, which is an adoption without modification of the identically titled CEI/IEC (Commission Électrotechnique Internationale/International Electrotechnical Commission) Standard 60601-2-33 (edition 2:2002 consolidated with amendment 1:2005). It supersedes the previous edition published in 1998 as CAN/CSA-C22.2 No. 601.2.33 (adopted CEI/IEC 601-2-33:1995).

INTRODUCTION

This Particular Standard is written at a moment in which the technical evolution of MR EQUIPMENT is in rapid progress and the scientific foundation of its safe use is still expanding.

The standard addresses technical aspects of the medical diagnostic MR SYSTEM and the MR EQUIPMENT therein, related to safety of PATIENTS examined with this system and personnel involved with its operation. Where limits of exposure of PATIENTS and medical staff are stated, these limits do not imply that such levels of exposure can be assumed to be acceptable for the population at large. Rather the implication is that the limits provide for the PATIENT a sensible balance between risk and benefit and for the medical staff a balanced risk, given their responsibility for the wellbeing of the PATIENT.

Organisational aspects of safety are the task of the USER. This task includes adequate training of staff, rules of access to the MR SYSTEM, qualification of staff for decisions that are related to safety, definition of medical responsibility and specific requirements for personnel following from that responsibility when the PATIENT is in or near the MR SYSTEM.

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Préface CSA

Ce document constitue la deuxième édition de la CAN/CSA-C22.2 nº 60601-2-33, Appareils électromédicaux - Partie 2-33 : Règles particulières de sécurité relatives aux appareils à résonance magnétique utilisés pour le diagnostic médical. II s'agit de l'adoption, sans modifications, de la norme CEI/IEC (Commission Électrotechnique Internationale/International Electrotechnical Commission) 60601-2-33 (édition 2:2002 consolidée par l'amendement 1:2005), qui porte le même titre. Cette norme remplace l'édition précédente publiée en 1998 qui portait la désignation CAN/CSA-C22.2 nº601.2.33 (norme CEI/IEC 601-2-33:1995 adoptée).

INTRODUCTION

La présente Norme Particulière est écrite à un moment où l'évolution technique des APPAREILS À RM est en rapide progrès et les fondements scientifiques de leur utilisation sûre sont constamment en évolution.

Cette norme traite des aspects techniques des SYSTÈMES À RM et des APPAREILS À RM destinés au diagnostic médical, relatifs à la sécurité des PATIENTS examinés avec ce système et du personnel associé à son fonctionnement. Lorsque les limites d'exposition des PATIENTS et du personnel médical sont établies, ces limites n'impliquent pas que de tels niveaux d'exposition puissent être considérés comme acceptables pour le grand public. Leur incidence réside davantage dans le fait que ces limites offrent au PATIENT un équilibre raisonnable entre les risques et les bénéfices, et au personnel médical un risque équilibré, compte tenu de sa responsabilité dans le bien-être du PATIENT.

Les aspects d'organisation de la sécurité relèvent de l'UTILISATEUR. Cette tâche comprend une formation appropriée du personnel, des règles d'accès aux SYSTÈMES À RM, une qualification du personnel concernant les décisions relatives à la sécurité, une définition de la responsabilité médicale et des exigences spécifiques pour le personnel en raison de la responsabilité qu'il a lorsque le PATIENT se trouve à l'intérieur ou à proximité du SYSTÈME À RM.

API RP 688 : Pulsation and Vibration Control in Positive Displacement Machinery Systems for Petroleum, Petrochemical, and Natural Gas Industry Services, First Edition

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The purpose of this document is to provide guidance on the application of pulsation and vibration control requirements found in the API purchasing specifications for positive displacement machinery. The fundamentals of pulsation and piping system analysis are presented in this Part.

The text begins with an overview of the fundamentals of pulsation and mechanical theory in Section 3. The intent of Section 3 is to introduce terminology and define the elements of the analysis process. Section 4 begins with a discussion of the acoustic and mechanical modeling techniques associated with the different design philosophies, which emphasize either pulsation or mechanical control, and concludes with a discussion on the appropriate selection of a Design Approach and Philosophy. Section 5 discusses the effects of pulsation on the accuracy of various types of flow measurement devices. Section 6 summarizes the requirements for documenting study results. Section 7 offers guidance on the performance of field testing to validate the results of the design process and to troubleshoot pulsation or vibration problems. Finally, methodologies for conducting a dynamic analysis of the compressor or pump valve performance are described in Section 8. The material in this Part is generally applicable to all types of positive displacement machinery.

Part 2 deals specifically with reciprocating compressors and provides commentary regarding each paragraph of Clause 7.9 of API 618, 5th Edition. It is the intent of the API Subcommittee on Mechanical Equipment that similar material be provided on reciprocating pumps and screw compressors in future editions.

AAMI/ISO 27185:2012 : Active implantable medical devices - Symbols to be used with cardiac device labels, labeling and information to be supplied by the manufacturer

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Identifies requirements for the development and use of symbols that may be used to convey information on the safe and effective use of cardiac rhythm management medical devices. The document is limited to symbols applicable to cardiac rhythm management medical devices that may be marketed globally. These symbols may be used on the device itself or its labels.

AAMI/IEC 601219E : Erratum for Medical electrical equipment - Part 2-19: Particular requirements for basic safety and essential performance of baby incubators

AAMI/IEC 601220E : Erratum for Medical electrical equipment - Part 2-20: Particular requirements for basic safety and essential performance of transport incubators

AAMI/IEC TIR61289:2011 : High frequency surgical equipment ? Operation and maintenance

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This technical report contains guidelines for medical and nursing personnel regarding the safe and effective operation of high frequency surgical equipment. This report will be of use to scientific/technical staff who may have responsibility for the maintenance of this equipment. This report deals with the safe operation of the high frequency surgical equipment, including the requirements outlined in ANSI/AAMI/IEC 60601-2-2:2009.

SMPTE ST 2065-1:2012 : Academy Color Encoding Specification (ACES)

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The specification defines the Academy Color Encoding Specification (ACES).

SMPTE ST 2065-2:2012 : Academy Printing Density (APD) ? Spectral Responsivities, Reference Measurement Device and Spectral Calculation

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This Standard defines Academy Printing Density (APD) by specifying the spectral responsivities and the APD reference measurement device.
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