{"id":373039,"date":"2024-10-20T02:32:03","date_gmt":"2024-10-20T02:32:03","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-iec-60601-2-832020a112021\/"},"modified":"2024-10-26T04:26:46","modified_gmt":"2024-10-26T04:26:46","slug":"bs-en-iec-60601-2-832020a112021","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-iec-60601-2-832020a112021\/","title":{"rendered":"BS EN IEC 60601-2-83:2020+A11:2021"},"content":{"rendered":"

Clause 1 of the general standard2<\/sup> applies, except as follows:<\/p>\n

201.1.1<\/b> Scope<\/p>\n

Replacement:<\/i><\/p>\n

This part of IEC 60601 is applicable to the basic safety<\/small> and essential performance<\/small> of home light therapy equipment<\/small>, intended for use in the home healthcare environment<\/small>. Home light therapy equipment<\/small> is typically used by a lay operator<\/small>.<\/p>\n

The scope of this document includes all light sources except laser.<\/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

201.1.2<\/b> Object<\/p>\n

Replacement:<\/i><\/p>\n

The object of this particular standard is to establish particular requirements for the basic safety<\/small> and essential performance<\/small> of home light therapy equipment<\/small>.<\/p>\n

201.1.3<\/b> Collateral standards<\/p>\n

Addition:<\/i><\/p>\n

This particular standard refers to those applicable collateral standards that are listed in Clause 2 of the general standard and Clause 201.2 of this particular standard.<\/p>\n

IEC 60601\u20111\u20112:2014, IEC 60601\u20111\u20116:2010 and IEC 60601\u20111\u20116:2010\/AMD1:2013 and IEC 60601\u20111\u201111:2015 apply as modified in Clauses 202, 206 and 211, respectively. IEC 60601\u20111\u20113, IEC 60601\u20111\u20118, IEC 60601\u20111\u201110 and IEC 60601\u20111\u201112 do not apply. All other published collateral standards in the IEC 60601\u20111 series apply as published.<\/p>\n

201.1.4<\/b> Particular standards<\/p>\n

Replacement:<\/i><\/p>\n

In the IEC 60601 series, particular standards may modify, replace or delete requirements contained in the general standard and collateral standards as appropriate for the particular me equipment<\/small> under consideration, and may add other basic safety<\/small> and essential performance<\/small> requirements.<\/p>\n

A requirement of a particular standard takes priority over the general standard.<\/p>\n

For brevity, IEC 60601\u20111:2005 and IEC 60601\u20111:2005\/AMD1:2012 are referred to in this particular standard as the general standard. Collateral standards are referred to by their document number.<\/p>\n

The numbering of clauses and subclauses of this particular standard corresponds to that of the general standard with the prefix “201” (e.g. 201.1 in this document addresses the content of Clause 1 of the general standard) or applicable collateral standard with the prefix “20x”, where x is the final digit(s) of the collateral standard document number (e.g. 202.4 in this particular standard addresses the content of Clause 4 of the IEC 60601\u20111\u20112 collateral standard, 203.4 in this particular standard addresses the content of Clause 4 of the IEC 60601\u20111\u20113 collateral standard, etc.). The changes to the text of the general standard are specified by the use of the following words:<\/p>\n

“Replacement”<\/i> means that the clause or subclause of the general standard or applicable collateral standard is replaced completely by the text of this particular standard.<\/p>\n

“Addition”<\/i> means that the text of this particular standard is additional to the requirements of the general standard or applicable collateral standard.<\/p>\n

“Amendment”<\/i> means that the clause or subclause of the general standard or applicable collateral standard is amended as indicated by the text of this particular standard.<\/p>\n

Subclauses, figures or tables which are additional to those of the general standard are numbered starting from 201.101. However, due to the fact that definitions in the general standard are numbered from 3.1 through 3.147, additional definitions in this document are numbered beginning from 201.3.201. Additional annexes are lettered AA, BB, etc., and additional items aa),<\/i> bb),<\/i> etc.<\/p>\n

Subclauses, figures or tables which are additional to those of a collateral standard are numbered starting from 20x, where “x” is the number of the collateral standard, e.g. 202 for IEC 60601\u20111\u20112, 203 forIEC 60601\u20111\u20113, etc.<\/p>\n

The term “this document” is used to make reference to the general standard, any applicable collateral standards and this particular standard taken together.<\/p>\n

Where there is no corresponding clause or subclause in this particular standard, the clause or subclause of the general standard or applicable collateral standard, although possibly not relevant, applies without modification; where it is intended that any part of the general standard or applicable collateral standard, although possibly relevant, is not to be applied, a statement to that effect is given in this particular standard.<\/p>\n

PDF Catalog<\/h4>\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
PDF Pages<\/th>\nPDF Title<\/th>\n<\/tr>\n
2<\/td>\nundefined <\/td>\n<\/tr>\n
6<\/td>\nAnnex ZA (normative)Normative references to international publications with their corresponding European publications <\/td>\n<\/tr>\n
14<\/td>\nEnglish
CONTENTS <\/td>\n<\/tr>\n
15<\/td>\nFOREWORD <\/td>\n<\/tr>\n
17<\/td>\nINTRODUCTION <\/td>\n<\/tr>\n
18<\/td>\n201.1 Scope, object and related standards <\/td>\n<\/tr>\n
19<\/td>\n201.2 Normative references <\/td>\n<\/tr>\n
20<\/td>\n201.3 Terms and definitions <\/td>\n<\/tr>\n
22<\/td>\n201.4 General requirements
201.5 General requirements for testing me equipment
201.6 Classification of me equipment and me systems <\/td>\n<\/tr>\n
23<\/td>\nTables
Table 201.101 \u2013 Emission limits for risk groups of home light therapy equipment <\/td>\n<\/tr>\n
24<\/td>\n201.7 Me equipment identification, marking and documents
Table 201.102 \u2013 Time criteria for risk groups of home light therapy equipment
Table 201.103 \u2013 Applicable angle of acceptance for the assessmentof emitted optical radiation from home light therapy equipment <\/td>\n<\/tr>\n
27<\/td>\n201.8 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
29<\/td>\n201.11 Protection against excessive temperatures and other hazards <\/td>\n<\/tr>\n
30<\/td>\n201.12 Accuracy of controls and instruments and protection against hazardous outputs
201.13 Hazardous situations and fault conditions for me equipment
201.14 Programmable electrical medical systems (pems)
201.15 Construction of me equipment
201.16 Me systems
201.17 Electromagnetic compatibility of me equipment and me systems
202 Electromagnetic disturbances \u2013 Requirements and tests <\/td>\n<\/tr>\n
31<\/td>\n206 Usability
211 Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment <\/td>\n<\/tr>\n
32<\/td>\nAnnexes <\/td>\n<\/tr>\n
33<\/td>\nAnnex C(informative)Guide to marking and labelling requirements for me equipment and me systems
Table 201.C.101 \u2013 Marking on the outside of me equipment, me systems or their parts <\/td>\n<\/tr>\n
34<\/td>\nTable 201.C.102 \u2013Safety signs per hazard and per risk group
Table 201.C.103 \u2013 Accompanying documents, instructions for use <\/td>\n<\/tr>\n
35<\/td>\nTable 201.C.104 \u2013Caution statements per hazard and per risk group <\/td>\n<\/tr>\n
36<\/td>\nAnnex D(informative)Symbols on marking
Table 201.D.1 \u2013 General symbols
Table 201.D.2 \u2013 Safety signs <\/td>\n<\/tr>\n
37<\/td>\nAnnex AA(informative)Particular guidance and rationale <\/td>\n<\/tr>\n
40<\/td>\nAnnex BB(informative)Protective eyewear for home light therapy equipment <\/td>\n<\/tr>\n
41<\/td>\nBibliography <\/td>\n<\/tr>\n
42<\/td>\nIndex of defined terms used in this particular standard <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":"

Medical electrical equipment – Particular requirements for the basic safety and essential performance of home light therapy equipment<\/b><\/p>\n\n\n\n\n
Published By<\/td>\nPublication Date<\/td>\nNumber of Pages<\/td>\n<\/tr>\n
BSI<\/b><\/a><\/td>\n2021<\/td>\n44<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n","protected":false},"featured_media":373048,"template":"","meta":{"rank_math_lock_modified_date":false,"ep_exclude_from_search":false},"product_cat":[144,2641],"product_tag":[],"class_list":{"0":"post-373039","1":"product","2":"type-product","3":"status-publish","4":"has-post-thumbnail","6":"product_cat-11-040-60","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\/373039","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\/373048"}],"wp:attachment":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/media?parent=373039"}],"wp:term":[{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product_cat?post=373039"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product_tag?post=373039"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}