{"id":278353,"date":"2024-10-19T18:45:35","date_gmt":"2024-10-19T18:45:35","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-iso-226752016-tc\/"},"modified":"2024-10-25T15:18:05","modified_gmt":"2024-10-25T15:18:05","slug":"bs-en-iso-226752016-tc","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-iso-226752016-tc\/","title":{"rendered":"BS EN ISO 22675:2016 – 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\n\n\n\n\n\n\n\n\n
PDF Pages<\/th>\nPDF Title<\/th>\n<\/tr>\n
114<\/td>\nEuropean foreword <\/td>\n<\/tr>\n
115<\/td>\nAnnex ZA (informative) Relationship between this European Standard and the Essential Requirements of EU Directive 93\/42\/EEC [OJ L 169] aimed to be covered
Table ZA.1 \u2014 Correspondence between this European standard and Annex I of Directive 93\/42\/EEC [OJ L 169] <\/td>\n<\/tr>\n
120<\/td>\nForeword <\/td>\n<\/tr>\n
121<\/td>\nIntroduction <\/td>\n<\/tr>\n
123<\/td>\n1 Scope
2 Normative references <\/td>\n<\/tr>\n
124<\/td>\n3 Terms and definitions
4 Designations and symbols of test forces <\/td>\n<\/tr>\n
125<\/td>\n5 Strength and related performance requirements and conditions of use <\/td>\n<\/tr>\n
126<\/td>\n6 Coordinate system and test configurations
6.1 General
6.2 Origin and axes of the coordinate system <\/td>\n<\/tr>\n
127<\/td>\n6.3 Reference points <\/td>\n<\/tr>\n
128<\/td>\n6.4 Test force F
6.5 Line of application of test force F
6.6 Lines of action of resultant reference forces FR1 and FR2
6.7 Longitudinal axis of the foot and effective ankle joint centre
6.7.1 General
6.7.2 Longitudinal axis of the foot <\/td>\n<\/tr>\n
129<\/td>\n6.7.3 Effective ankle-joint centre, CA <\/td>\n<\/tr>\n
130<\/td>\n7 Test loading conditions and test loading levels
7.1 Test loading conditions
7.2 Test loading levels <\/td>\n<\/tr>\n
131<\/td>\n8 Values of test forces, dimensions and cycles <\/td>\n<\/tr>\n
138<\/td>\n9 Compliance
9.1 General <\/td>\n<\/tr>\n
139<\/td>\n9.2 Particular arrangements and requirements concerning the part required to connect an ankle-foot device or foot unit to the remainder of a prosthetic structure
9.2.1 Arrangements for testing
9.2.2 Requirements for claiming compliance
9.3 Number of tests and test samples required to claim compliance with this International Standard <\/td>\n<\/tr>\n
140<\/td>\n9.4 Multiple use of test samples
9.4.1 General
9.4.2 Restriction
9.5 Testing at particular test loading levels not specified in this International Standard <\/td>\n<\/tr>\n
141<\/td>\n10 Test samples
10.1 Selection of test samples
10.1.1 General
10.1.2 Selection of ankle-foot devices and foot units of appropriate size of foot <\/td>\n<\/tr>\n
142<\/td>\n10.2 Types of test sample
10.2.1 Complete structure
10.2.2 Partial structure
10.3 Preparation of test samples <\/td>\n<\/tr>\n
143<\/td>\n10.4 Identification of test samples
10.5 Alignment of test samples
10.6 Worst-case alignment position of test samples <\/td>\n<\/tr>\n
145<\/td>\n11 Responsibility for test preparation <\/td>\n<\/tr>\n
146<\/td>\n12 Test submission document
12.1 General requirements
12.2 Information required for test samples <\/td>\n<\/tr>\n
147<\/td>\n12.3 Information required for tests
12.3.1 General
12.3.2 For all tests
12.3.3 For the static proof test and the static ultimate strength test
12.3.4 For the static ultimate strength test
12.3.5 For the cyclic test <\/td>\n<\/tr>\n
148<\/td>\n13 Equipment
13.1 General
13.2 End attachments
13.2.1 General
13.2.2 Proof test of end attachments <\/td>\n<\/tr>\n
150<\/td>\n13.3 Jig (optional) <\/td>\n<\/tr>\n
151<\/td>\n13.4 Test equipment
13.4.1 Test equipment to perform static heel and forefoot loading <\/td>\n<\/tr>\n
152<\/td>\n13.4.2 Test equipment to perform cyclic loading <\/td>\n<\/tr>\n
159<\/td>\n14 Accuracy
14.1 General
14.2 Accuracy of equipment
14.3 Accuracy of procedure <\/td>\n<\/tr>\n
160<\/td>\n15 Test principles
15.1 General <\/td>\n<\/tr>\n
161<\/td>\n15.2 Static test procedure
15.3 Cyclic test procedure
16 Test procedures
16.1 Test loading requirements
16.1.1 Preparation for test loading <\/td>\n<\/tr>\n
165<\/td>\n16.1.2 Test loading conditions
16.2 Static proof test
16.2.1 Test method <\/td>\n<\/tr>\n
167<\/td>\n16.2.2 Performance requirement
16.2.3 Compliance conditions <\/td>\n<\/tr>\n
169<\/td>\n16.3 Static ultimate strength test
16.3.1 Test method <\/td>\n<\/tr>\n
172<\/td>\n16.3.2 Performance requirements
16.3.3 Compliance conditions <\/td>\n<\/tr>\n
173<\/td>\n16.4 Cyclic test
16.4.1 Test method <\/td>\n<\/tr>\n
176<\/td>\n16.4.2 Performance requirements <\/td>\n<\/tr>\n
177<\/td>\n16.4.3 Compliance conditions <\/td>\n<\/tr>\n
179<\/td>\n17 Test laboratory\/facility log
17.1 General requirements
17.2 Specific requirements
18 Test report
18.1 General requirements <\/td>\n<\/tr>\n
180<\/td>\n18.2 Specific requirements
18.3 Options
19 Classification and designation
19.1 General
19.2 Examples of classification and designation <\/td>\n<\/tr>\n
181<\/td>\n20 Labelling
20.1 General <\/td>\n<\/tr>\n
182<\/td>\n20.2 Use of mark \u201c*)\u201d and warning symbol
20.3 Examples of label layout <\/td>\n<\/tr>\n
183<\/td>\n20.4 Label placement <\/td>\n<\/tr>\n
184<\/td>\nAnnex\u00a0A (informative) Reference data for the specification of the test loading conditions and\u00a0test loading levels of this International Standard <\/td>\n<\/tr>\n
192<\/td>\nAnnex\u00a0B (informative) Guidance on the application of an alternative static ultimate strength test <\/td>\n<\/tr>\n
193<\/td>\nAnnex\u00a0C (normative) Application of an additional test loading level P6, P7, and P8 <\/td>\n<\/tr>\n
195<\/td>\nAnnex\u00a0D (informative) Summary of the records to be entered in the test laboratory\/facility log <\/td>\n<\/tr>\n
201<\/td>\nAnnex\u00a0E (informative) Information on Technical Report ISO\/TR\u00a022676[[1]] <\/td>\n<\/tr>\n
212<\/td>\nAnnex\u00a0F (informative) Reference to the essential principles of safety and performance of medical devices according to ISO\/TR\u00a016142 <\/td>\n<\/tr>\n
213<\/td>\nBibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":"

Tracked Changes. Prosthetics. Testing of ankle-foot devices and foot units. Requirements and test methods<\/b><\/p>\n\n\n\n\n
Published By<\/td>\nPublication Date<\/td>\nNumber of Pages<\/td>\n<\/tr>\n
BSI<\/b><\/a><\/td>\n2020<\/td>\n216<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n","protected":false},"featured_media":278354,"template":"","meta":{"rank_math_lock_modified_date":false,"ep_exclude_from_search":false},"product_cat":[141,2641],"product_tag":[],"class_list":{"0":"post-278353","1":"product","2":"type-product","3":"status-publish","4":"has-post-thumbnail","6":"product_cat-11-040-40","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\/278353","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\/278354"}],"wp:attachment":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/media?parent=278353"}],"wp:term":[{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product_cat?post=278353"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product_tag?post=278353"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}