{"id":9831,"date":"2026-02-24T15:11:44","date_gmt":"2026-02-24T07:11:44","guid":{"rendered":"https:\/\/www.packqc.com\/standard\/iso-17218\/"},"modified":"2026-03-12T16:59:48","modified_gmt":"2026-03-12T08:59:48","slug":"iso-17218","status":"publish","type":"standard","link":"https:\/\/www.packqc.com\/et\/standard\/iso-17218\/","title":{"rendered":"ISO 17218"},"content":{"rendered":"<h2 class=\"wp-block-heading\">Mis on ISO 17218?<\/h2>\n\n\n\n<p>ISO 17218, pealkirjaga <em data-start=\"1045\" data-end=\"1091\">\u201cSteriilsed akupunktuuri n\u00f5elad \u00fchekordseks kasutamiseks\u201d<\/em>, kirjeldab akupunktuurin\u00f5elte hindamise standardiseeritud meetodeid. Selle peamine eesm\u00e4rk on tagada, et n\u00f5elad on kliinilisel kasutamisel ohutud, t\u00f5husad ja usaldusv\u00e4\u00e4rsed. Standard sisaldab suuniseid testimiseks <strong data-start=\"1302\" data-end=\"1322\">n\u00f5ela intensiivsus<\/strong>, <strong data-start=\"1324\" data-end=\"1344\">n\u00f5ela teravus<\/strong>ja <strong data-start=\"1350\" data-end=\"1381\">n\u00f5ela l\u00e4bitorkamise j\u00f5udlus<\/strong> kinnitamaks, et n\u00f5elad vastavad \u00fclemaailmsetele kvaliteedistandarditele.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Akupunktuuri n\u00f5eltesti selgitamine<\/h2>\n\n\n\n<p>Standard m\u00e4\u00e4rab kindlaks meetodid kolme olulise katseaspekti jaoks:<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">1. N\u00f5ela intensiivsuse testimine<\/h3>\n\n\n\n<p>N\u00f5ela intensiivsus m\u00f5\u00f5dab n\u00f5ela otsa v\u00f5imet vastu seista paindumisele v\u00f5i purunemisele. ISO 17218 kohaselt t\u00e4hendab see, et akupunktuurin\u00f5el asetatakse vertikaalselt vastu terasplokki. J\u00f5udu suurendatakse j\u00e4rk-j\u00e4rgult, kuni see vastab punktis 5.3.5.2 esitatud arvulistele kriteeriumidele. P\u00e4rast koormuse hoidmist (5-10) sekundit kontrollitakse n\u00f5ela otsa 5-kordse suurendusega. N\u00f5el peab j\u00e4\u00e4ma sirgeks, ilma paindumise v\u00f5i konksuta, tagades, et see ei deformeeru tegeliku n\u00f5elravi ajal.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">2. N\u00f5ela teravuse testimine<\/h3>\n\n\n\n<p>Teravuse testimisel hinnatakse j\u00f5udu, mida n\u00f5ela ots vajab alumiiniumfooliumi l\u00e4bistamiseks. P\u00e4rast intensiivsuse katsetamist j\u00e4\u00e4b sama n\u00f5el seadmesse kinnitatud akupunktuurin\u00f5el. Seej\u00e4rel surutakse n\u00f5el vastu alumiiniumfooliumi, kuni see l\u00e4bistab seda. Seade registreerib automaatselt l\u00e4bistamisj\u00f5u, andes kvantitatiivseid andmeid n\u00f5ela teravuse kohta. Korralikult terav n\u00f5el vajab fooliumi l\u00e4bistamiseks v\u00e4hem j\u00f5udu, mis n\u00e4itab selle sujuvat ja t\u00e4pset l\u00e4bistamisv\u00f5imet.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">3. N\u00f5elapunktuuride testimine<\/h3>\n\n\n\n<p>Punktsioonitestiga hinnatakse, kui h\u00e4sti tungib n\u00f5el pehmete kudede v\u00f5i materjalide sisse. ISO 17218 n\u00e4eb ette kaks meetodit:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong data-start=\"2753\" data-end=\"2786\">Kvalitatiivne meetod (meetod A)<\/strong>: Selleks kasutatakse kirurgilistest kummikindadest (ISO 10282 n\u00f5uetele vastavat) membraani, mis on pingutatud \u00fcle tassi. N\u00f5el surutakse vertikaalselt membraani sisse. Kui m\u00f5lk on minimaalne ja vastupanu v\u00e4ike, on n\u00f5el terav. See meetod v\u00f5imaldab kiiret visuaalset kontrolli teravuse j\u00e4rjepidevuse \u00fcle.<\/li>\n\n\n\n<li><strong data-start=\"3074\" data-end=\"3108\">Kvantitatiivne meetod (meetod B)<\/strong>: Selleks kasutatakse pol\u00fcmeeritud pol\u00fcuretaankile paksusega (0,35 \u00b1 0,05) mm ja Shore'i k\u00f5vadusega (85 \u00b1 10) Shore A. N\u00f5ela liigutatakse kiirusega 100 mm\/min, samal ajal kui registreeritakse l\u00e4bistamisj\u00f5ud ja nihkumine. P\u00f5hij\u00f5u v\u00e4\u00e4rtused F0F_0F0, F1F_1F1 ja F2F_2F2 kajastavad n\u00f5ela l\u00e4bistamise ja h\u00f5\u00f5rdumise omadusi. See meetod annab v\u00e4ga usaldusv\u00e4\u00e4rseid andmeid, et hinnata punktsiooniv\u00f5imet ja v\u00f5rrelda erinevaid n\u00f5elu.<\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">ISO 17218 n\u00f5uetele vastavuse parimad tavad<\/h2>\n\n\n\n<p>Kvaliteedikontrolli- ja testimismeeskonnad peaksid hoolikalt:<\/p>\n\n\n\n<p>\u2705 Kasutage standardiseeritud katseseadmeid, et korrata <a href=\"https:\/\/www.iso.org\/standard\/59443.html\" target=\"_blank\" rel=\"noopener nofollow\">ISO 17218<\/a>\u2019tingimused<br data-start=\"3728\" data-end=\"3731\">\u2705 Registreerige katseandmed t\u00e4pselt, sealhulgas k\u00f5ik j\u00f5umuutused punktsioonikatsete ajal.<br data-start=\"3822\" data-end=\"3825\">\u2705 V\u00f5rdle tulemusi teadaolevate kvaliteedin\u00f5elte tulemuslikkuse v\u00f5rdlemiseks.<br data-start=\"3903\" data-end=\"3906\">\u2705 dokumenteerida ja arhiveerida katsetulemused j\u00e4lgitavuse ja regulatiivse vastavuse tagamiseks.<\/p>\n\n\n\n<p>Neid tavasid j\u00e4rgides saavad tootjad ja kvaliteedikontrolli t\u00f6\u00f6tajad oma n\u00f5elasid kindlalt hinnata.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">\n\t\t\t\tV\u00f5tke meiega \u00fchendust Hankige ISO 17218 testimise lahendus\t\t\t\t<\/h2>\n\n\n\n<p>Kell <strong data-start=\"4163\" data-end=\"4183\">Rakuinstrumendid<\/strong>, oleme spetsialiseerunud rahvusvahelistele standarditele, nagu ISO 17218, vastavate katseseadmete projekteerimisele ja tootmisele. Meie seadmed tagavad t\u00e4pse <strong data-start=\"4338\" data-end=\"4421\">n\u00f5ela intensiivsuse testimine, n\u00f5ela teravuse testimine ja n\u00f5ela l\u00e4bistamise testimine<\/strong>. Pakume ka kohandatud testimislahendusi erin\u00f5uete jaoks, mis v\u00f5imaldab teil t\u00e4ita arenevaid turun\u00f5udeid t\u00e4psuse ja usaldusv\u00e4\u00e4rsusega.<\/p>\n\n\n\n<p>Olgu tegemist siis pakendite, meditsiiniseadmete v\u00f5i akupunktuuri n\u00f5elte testimisega, <strong data-start=\"4642\" data-end=\"4662\">Rakuinstrumendid<\/strong> omab teadmisi, mis aitavad teil s\u00e4ilitada kvaliteeti, ohutust ja n\u00f5uetele vastavust.<\/p>\n\n\n\n<p><\/p>","protected":false},"excerpt":{"rendered":"<p>What is ISO 17218? ISO 17218, titled \u201cSterile acupuncture needles for single use\u201d, outlines standardized methods for evaluating acupuncture needles. Its main purpose is to ensure that needles are safe, effective, and reliable during clinical use. The standard includes guidelines for testing needle intensity, needle sharpness, and needle puncture performance to confirm that the needles [&hellip;]<\/p>","protected":false},"featured_media":5491,"parent":0,"template":"","meta":{"_acf_changed":true,"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"set","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""}}},"standard-category":[],"class_list":["post-9831","standard","type-standard","status-publish","has-post-thumbnail","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.packqc.com\/et\/wp-json\/wp\/v2\/standard\/9831","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.packqc.com\/et\/wp-json\/wp\/v2\/standard"}],"about":[{"href":"https:\/\/www.packqc.com\/et\/wp-json\/wp\/v2\/types\/standard"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.packqc.com\/et\/wp-json\/wp\/v2\/media\/5491"}],"wp:attachment":[{"href":"https:\/\/www.packqc.com\/et\/wp-json\/wp\/v2\/media?parent=9831"}],"wp:term":[{"taxonomy":"standard-category","embeddable":true,"href":"https:\/\/www.packqc.com\/et\/wp-json\/wp\/v2\/standard-category?post=9831"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}