{"id":386872,"date":"2024-10-20T03:37:28","date_gmt":"2024-10-20T03:37:28","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-iso-80601-2-742021-tc\/"},"modified":"2024-10-26T06:37:29","modified_gmt":"2024-10-26T06:37:29","slug":"bs-en-iso-80601-2-742021-tc","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-iso-80601-2-742021-tc\/","title":{"rendered":"BS EN ISO 80601-2-74:2021 – TC"},"content":{"rendered":"

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\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
PDF Pages<\/th>\nPDF Title<\/th>\n<\/tr>\n
1<\/td>\n30447149 <\/td>\n<\/tr>\n
123<\/td>\nA-30425917 <\/td>\n<\/tr>\n
124<\/td>\nundefined <\/td>\n<\/tr>\n
126<\/td>\nEuropean foreword
Endorsement notice <\/td>\n<\/tr>\n
129<\/td>\nForeword <\/td>\n<\/tr>\n
131<\/td>\nIntroduction <\/td>\n<\/tr>\n
133<\/td>\n201.1 Scope, object and related standards <\/td>\n<\/tr>\n
135<\/td>\n201.2 Normative references <\/td>\n<\/tr>\n
137<\/td>\n201.3 Terms and definitions <\/td>\n<\/tr>\n
140<\/td>\n201.4 General requirements <\/td>\n<\/tr>\n
143<\/td>\n201.5 General requirements for testing of ME equipment <\/td>\n<\/tr>\n
144<\/td>\n201.6 Classification of ME equipment and ME systems <\/td>\n<\/tr>\n
145<\/td>\n201.7 ME equipment identification, marking and documents <\/td>\n<\/tr>\n
152<\/td>\n201.8 Protection against electrical hazards form ME equipment
201.9 Protection against mechanical hazards of ME equipment and ME systems <\/td>\n<\/tr>\n
153<\/td>\n201.10 Protection against unwanted and excessive radiation hazards
201.11 Protection against excessive temperatures and other hazards <\/td>\n<\/tr>\n
156<\/td>\n201.12 Accuracy of controls and instruments and protection against hazardous outputs <\/td>\n<\/tr>\n
162<\/td>\n201.13 Hazardous situations and fault conditions for ME Equipment <\/td>\n<\/tr>\n
163<\/td>\n201.14 Programmable electrical medical systems (PEMS) <\/td>\n<\/tr>\n
164<\/td>\n201.15 Construction of ME equipment
201.16 ME systems
201. 16.2 Accompanying documents of an ME system
201.17 Electromagnetic compatibility of ME equipment and ME systems <\/td>\n<\/tr>\n
165<\/td>\n201.101 Breathing system connectors and ports <\/td>\n<\/tr>\n
167<\/td>\n201.102 Requirements for the breathing system and accessories <\/td>\n<\/tr>\n
168<\/td>\n201.103 Liquid container
201.104 Functional connection <\/td>\n<\/tr>\n
169<\/td>\n202 Electromagnetic disturbances \u2014 Requirements and tests <\/td>\n<\/tr>\n
170<\/td>\n206 Usability <\/td>\n<\/tr>\n
171<\/td>\n208 General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
211 Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment <\/td>\n<\/tr>\n
172<\/td>\nAnnex C (informative) Guide to marking and labelling requirements for ME equipment and ME systems <\/td>\n<\/tr>\n
177<\/td>\nAnnex D (informative) Symbols on marking <\/td>\n<\/tr>\n
179<\/td>\nAnnex AA (informative) Particular guidance and rationale <\/td>\n<\/tr>\n
196<\/td>\nAnnex BB (normative) * Determination of the accuracy of the displayed measured gas temperature <\/td>\n<\/tr>\n
198<\/td>\nAnnex CC (normative) * Determination of the humidification output <\/td>\n<\/tr>\n
203<\/td>\nAnnex DD (normative) * Specific enthalpy calculations <\/td>\n<\/tr>\n
205<\/td>\nAnnex EE (normative) Removable temperature sensors and mating ports <\/td>\n<\/tr>\n
209<\/td>\nAnnex FF (normative) * Reference temperature sensor <\/td>\n<\/tr>\n
212<\/td>\nAnnex GG (informative) Saturation vapour pressure <\/td>\n<\/tr>\n
213<\/td>\nAnnex HH (informative) Reference to the IMDRF essential principles and labelling guidances <\/td>\n<\/tr>\n
217<\/td>\nAnnex II (informative) Reference to the essential principles of safety and performance of medical devices in accordance with ISO 16142-1:2016 <\/td>\n<\/tr>\n
220<\/td>\nAnnex JJ (informative) Reference to the general safety and performance requirements <\/td>\n<\/tr>\n
223<\/td>\nAnnex KK (informative) Terminology \u2014 Alphabetized index of defined terms <\/td>\n<\/tr>\n
227<\/td>\nBibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":"

Tracked Changes. Medical electrical equipment – Particular requirements for basic safety and essential performance of respiratory humidifying 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>\n232<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n","protected":false},"featured_media":386880,"template":"","meta":{"rank_math_lock_modified_date":false,"ep_exclude_from_search":false},"product_cat":[137,2641],"product_tag":[],"class_list":{"0":"post-386872","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\/386872","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\/386880"}],"wp:attachment":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/media?parent=386872"}],"wp:term":[{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product_cat?post=386872"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product_tag?post=386872"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}