{"id":277880,"date":"2024-10-19T18:43:10","date_gmt":"2024-10-19T18:43:10","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-iso-80601-2-552018\/"},"modified":"2024-10-25T15:14:41","modified_gmt":"2024-10-25T15:14:41","slug":"bs-en-iso-80601-2-552018","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-iso-80601-2-552018\/","title":{"rendered":"BS EN ISO 80601-2-55:2018"},"content":{"rendered":"
IEC 60601-1:2005+Amd 1:2012, Clause 1 applies, except as follows:<\/p>\n
201.1.1<\/b> *Scope<\/p>\n
IEC 60601-1:2005+Amd 1:2012, 1.1 is replaced by:<\/p>\n
This document specifies particular requirements for the basic safety<\/small> and essential performance<\/small> of a respiratory gas monitor<\/small> (rgm<\/small>), hereafter referred to as me equipment<\/small>, intended for continuous operation<\/small> for use with a patient<\/small>.<\/p>\n
This document specifies requirements for<\/p>\n
anaesthetic gas monitoring,<\/p>\n<\/li>\n
carbon dioxide monitoring, and<\/p>\n<\/li>\n
oxygen monitoring.<\/p>\n<\/li>\n<\/ul>\n
\nNOTE 1 An rgm<\/small> can be either stand-alone me equipment<\/small> or integrated into other equipment, e.g. an anaesthetic workstation or a ventilator.<\/p>\n<\/blockquote>\n
This document is not applicable to an RGM intended for use with flammable anaesthetic agents.<\/p>\n
If a clause or subclause is specifically intended to be applicable to me equipment<\/small> only or to me systems<\/small> 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<\/small> and to me systems<\/small>, as relevant.<\/p>\n
hazards<\/small> inherent in the intended physiological function of me equipment<\/small> or me systems<\/small> within the scope of this document are not covered by specific requirements in this document except in IEC 60601-1:2005+Amd 1:2012, 7.2.13 and 8.4.1.<\/p>\n
\nNOTE 2 Additional information can be found in IEC 60601-1:2005+Amd 1:2012, 4.2.<\/p>\n<\/blockquote>\n
201.1.2<\/b> Object<\/p>\n
IEC 60601-1:2005+Amd 1:2012, 1.2 is replaced by:<\/p>\n
The object of this document is to establish particular basic safety<\/small> and essential performance<\/small> requirements for an rgm<\/small> (as defined in 201.3.210) and its accessories<\/small>.<\/p>\n
\nNOTE accessories<\/small> are included because the combination of the rgm<\/small> and the accessories<\/small> needs to be safe. accessories<\/small> can have a significant impact on the basic safety<\/small> and essential performance<\/small> of an rgm<\/small>.<\/p>\n<\/blockquote>\n
201.1.3<\/b> Collateral standards<\/p>\n
IEC 60601-1:2005+Amd 1:2012, 1.3 applies with the following addition:<\/p>\n
This document refers to those applicable collateral standards that are listed in IEC 60601-1:2005+Amd 1:2012, Clause 2, as well as those listed in 201.2 of this document and to the following exceptions:<\/p>\n
IEC 60601-1-3:2008 and IEC 60601-1-9:2007+Amd 1:2013 do not apply.<\/p>\n
201.1.4<\/b> Particular standards<\/p>\n
IEC 60601-1:2005+Amd 1:2012, 1.4 is replaced by:<\/p>\n
In the IEC 60601 series, particular standards can modify, replace or delete requirements contained in the general standard, including the collateral standards, as appropriate for the particular me equipment<\/small> under consideration, and may add other basic safety<\/small> or essential performance<\/small> requirements.<\/p>\n
A requirement of a particular standard takes priority over IEC 60601-1:2005+Amd 1:2012 or the collateral standards.<\/p>\n
For brevity, IEC 60601-1:2005+Amd 1:2012 is referred to in this document as the general standard. Collateral standards are referred to by their document number.<\/p>\n
The numbering of clauses and subclauses of this document corresponds to those of the general standard with the prefix \u201c201\u201d (e.g. 201.1 in this document addresses the content of Clause 1 of the general standard) or applicable collateral standard with the prefix \u201c2xx\u201d where xx is the final digits of the collateral standard document number (e.g. 202.4 addresses the content of IEC 60601-1-2, Clause 4 collateral standard, 208.4 addresses the content of IEC 60601-1-8, Clause 4 collateral standard, etc.). The changes to the text of the general standard are specified by the use of the following words:<\/p>\n
\n
- \n
\u201cReplacement\u201d means that the clause or subclause of IEC 60601-1:2005+Amd 1:2012 or the applicable collateral standard is replaced completely by the text of this document.<\/p>\n<\/li>\n
- \n
\u201cAddition\u201d means that the text of this document is additional to the requirements of IEC 60601-1:2005+Amd 1:2012 or the applicable collateral standard.<\/p>\n<\/li>\n
- \n
\u201cAmendment\u201d means that the clause or subclause of IEC 60601-1:2005+Amd 1:2012 or the applicable collateral standard is amended as indicated by the text of this document.<\/p>\n<\/li>\n<\/ul>\n
Subclauses or figures that are additional to those of the general standard are numbered starting from 201.101, additional annexes are lettered AA, BB, etc., and additional items aa), bb), etc.<\/p>\n
Subclauses or figures that are additional to those of a collateral standard are numbered starting from 20x, where \u201cx\u201d is the number of the collateral standard, e.g. 202 for IEC 60601-1-2, 203 for IEC 60601-1-3, etc.<\/p>\n
The term \u201cthis standard\u201d is used to make reference to IEC 60601-1:2005+Amd 1:2012, any applicable collateral standards, and this document taken together.<\/p>\n
Where there is no corresponding clause or subclause in this document, the clause or subclause of IEC 60601-1:2005+Amd 1:2012 or the applicable collateral standard, although possibly not relevant, applies without modification; where it is intended that any part of IEC 60601-1:2005+Amd 1:2012 or the applicable collateral standard, although possibly relevant, is not to be applied, a statement to that effect is given in this document.<\/p>\n
PDF Catalog<\/h4>\n
\n
\n PDF Pages<\/th>\n PDF Title<\/th>\n<\/tr>\n \n 2<\/td>\n undefined <\/td>\n<\/tr>\n \n 7<\/td>\n Annex ZA(informative)Relationship between this European Standard and the essential requirements of Directive 93\/42\/EEC [OJ L 169] aimed to be covered <\/td>\n<\/tr>\n \n 17<\/td>\n 201.1 Scope, object and related standards
201.1.1 *Scope
201.1.2 Object <\/td>\n<\/tr>\n\n 18<\/td>\n 201.1.3 Collateral standards
201.1.4 Particular standards <\/td>\n<\/tr>\n\n 19<\/td>\n 201.2 Normative references <\/td>\n<\/tr>\n \n 20<\/td>\n 201.3 Terms and definitions <\/td>\n<\/tr>\n \n 22<\/td>\n 201.4 General requirements <\/td>\n<\/tr>\n \n 23<\/td>\n 201.5 General requirements for testing of me equipment
201.6 Classification of me equipment and me systems
201.7 Me equipment identification, marking, and documents <\/td>\n<\/tr>\n\n 29<\/td>\n 201.8 Protection against electrical hazards from me equipment
201.9 Protection against mechanical hazards of ME equipment and ME systems
201.10 Protection against unwanted and excessive radiation hazards <\/td>\n<\/tr>\n\n 30<\/td>\n 201.11 Protection against excessive temperatures and other hazards <\/td>\n<\/tr>\n \n 32<\/td>\n 201.12 Accuracy of controls and instruments and protection against hazardous outputs <\/td>\n<\/tr>\n \n 38<\/td>\n 201.13 Hazardous situations and fault conditions
201.14 Programmable electrical medical systems (pems)
201.15 Construction of me equipment <\/td>\n<\/tr>\n\n 40<\/td>\n 201.16 Me systems
201.17 Electromagnetic compatibility of me equipment and me systems
201.101 *Interfering gas and vapour effects <\/td>\n<\/tr>\n\n 41<\/td>\n 201.102 *Gas leakage
201.103 *Port connectors for diverting rgms
201.104 *Sampling flowrate
201.105 *Contamination of breathing systems
201.106 Functional connection <\/td>\n<\/tr>\n\n 43<\/td>\n 202 Electromagnetic disturbances \u2014 Requirements and tests
206 Usability <\/td>\n<\/tr>\n\n 44<\/td>\n 208 General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems <\/td>\n<\/tr>\n \n 46<\/td>\n 211 General requirements, tests and guidance for medical electrical equipment and medical electrical systems used in the home healthcare environment
212 General requirements, tests and guidance for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":"Medical electrical equipment – Particular requirements for the basic safety and essential performance of respiratory gas monitors<\/b><\/p>\n
\n\n
\n Published By<\/td>\n Publication Date<\/td>\n Number of Pages<\/td>\n<\/tr>\n \n BSI<\/b><\/a><\/td>\n 2018<\/td>\n 76<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n","protected":false},"featured_media":277884,"template":"","meta":{"rank_math_lock_modified_date":false,"ep_exclude_from_search":false},"product_cat":[137,2641],"product_tag":[],"class_list":{"0":"post-277880","1":"product","2":"type-product","3":"status-publish","4":"has-post-thumbnail","6":"product_cat-11-040-10","7":"product_cat-bsi","9":"first","10":"instock","11":"sold-individually","12":"shipping-taxable","13":"purchasable","14":"product-type-simple"},"_links":{"self":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product\/277880","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/types\/product"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/media\/277884"}],"wp:attachment":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/media?parent=277880"}],"wp:term":[{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product_cat?post=277880"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product_tag?post=277880"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}