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.srx-certs .srx-hl-item{flex-direction:row;align-items:flex-start;gap:16px}\n  .srx-certs .srx-c-controls{padding:18px}\n  .srx-certs .sct-filters button{flex:1 1 auto}\n  .srx-certs a.srx-pill{width:100%;justify-content:center}\n}\n\n.srx-certs .srx-c-plate{display:flex;align-items:center;justify-content:center;width:132px;height:56px;flex:none;padding:8px 14px;background:#fff;border:1px solid #E7EFF5;border-radius:12px;box-shadow:inset 0 1px 0 #fff,0 1px 2px rgba(16,42,60,.04)}\n.srx-certs .srx-c-plate img{display:block;width:auto;height:auto;max-width:104px;max-height:40px;object-fit:contain}\n\n.srx-certs .srx-c-gatenote{margin:10px 0 0;font-size:14.5px;color:#5B6D79}\n\n#suresult-certifications-trust-center {letter-spacing:0}\n#suresult-certifications-trust-center .srx-cert-facts {margin:16px 0 24px;font-size:14px;line-height:1.55;display:grid;grid-template-columns:1fr;gap:2px}\n#suresult-certifications-trust-center .srx-cert-facts dt {font-weight:600;color:#4b5563;margin:10px 0 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.srx-cert-faq p {max-width:800px;margin:14px 0 0;line-height:1.7}\n#suresult-certifications-trust-center [hidden] {display:none!important}\n<\/style>\n<div class=\"srx-certs\" id=\"suresult-certifications-trust-center\">\n<!-- 1. MASTHEAD -->\n<section class=\"srx-c-sec\">\n<div class=\"srx-eyebrow\">Suresult Trust Center<\/div>\n<div class=\"srx-t-title\">Ultrasound Certifications &amp; Regulatory Documents<\/div>\n<p class=\"srx-lead\">Review Suresult wireless ultrasound documentation for the D, L and C series. This library brings together regulatory records, the EU Declaration of Conformity, quality management certificates, and technical and market documentation summaries. Each entry identifies the document type, reference and product family; full PDFs are available after sign-in.<\/p>\n<p class=\"srx-c-meta\">11 documents available | Library updated: <time datetime=\"2026-09-05\">September 5, 2026<\/time><\/p>\n<ul aria-label=\"Compliance highlights\" class=\"srx-hl\">\n<li class=\"srx-hl-item\">\n<span class=\"srx-c-plate\"><img alt=\"FDA logo\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/suresultmed.com\/wp-content\/uploads\/2025\/02\/fda-logo-icon.png\"\/><\/span>\n<div>\n<div class=\"srx-hl-label\">FDA 510(k)<\/div>\n<div class=\"srx-hl-text\">Wireless probe ultrasound scanner documentation available for buyer review.<\/div>\n<\/div>\n<\/li>\n<li class=\"srx-hl-item\">\n<span class=\"srx-c-plate\"><img alt=\"Health Canada logo\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/3\/3f\/Health_Canada_logo.svg\"\/><\/span>\n<div>\n<div class=\"srx-hl-label\">Canada \/ Health Canada<\/div>\n<div class=\"srx-hl-text\">Medical device license documentation available for buyer review.<\/div>\n<\/div>\n<\/li>\n<li class=\"srx-hl-item\">\n<span class=\"srx-c-plate\"><img alt=\"CE marking\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/suresultmed.com\/wp-content\/uploads\/2025\/02\/ce-logo-icon.webp\"\/><\/span>\n<div>\n<div class=\"srx-hl-label\">EU MDR \/ CE<\/div>\n<div class=\"srx-hl-text\">European conformity and MDR-related quality documentation.<\/div>\n<\/div>\n<\/li>\n<li class=\"srx-hl-item\">\n<span class=\"srx-c-plate\"><img alt=\"ISO logo\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/e\/e3\/ISO_Logo_%28Red_square%29.svg\"\/><\/span>\n<div>\n<div class=\"srx-hl-label\">ISO 13485 QMS<\/div>\n<div class=\"srx-hl-text\">Quality management system documentation for medical devices.<\/div>\n<\/div>\n<\/li>\n<li class=\"srx-hl-item\">\n<span class=\"srx-med srx-med--seal\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-globe\"><\/use><\/svg><\/span>\n<div>\n<div class=\"srx-hl-label\">Global Documentation<\/div>\n<div class=\"srx-hl-text\">Regional registrations, safety evidence, and supporting summaries.<\/div>\n<\/div>\n<\/li>\n<li class=\"srx-hl-item\">\n<span class=\"srx-c-plate\"><img alt=\"Therapeutic Goods Administration logo\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/www.tga.gov.au\/sites\/default\/files\/2025-05\/DHAC-TGA-strip-logo-black-730x151.png\"\/><\/span>\n<div>\n<div class=\"srx-hl-label\">Australia \/ TGA<\/div>\n<div class=\"srx-hl-text\">ARTG medical device registration documentation for buyer review.<\/div>\n<\/div>\n<\/li>\n<\/ul>\n<hr class=\"srx-c-rule\"\/>\n<\/section>\n<!-- 2. CERTIFICATE LIBRARY -->\n<section aria-labelledby=\"sct-library-title\" class=\"srx-c-sec\">\n<div class=\"srx-c-head\">\n<div class=\"srx-c-head-main\">\n<div class=\"srx-eyebrow\">Certificate library<\/div>\n<h2 id=\"sct-library-title\">Documentation Available for Buyer Review<\/h2>\n<p class=\"srx-c-intro\">Review documents by market, standard or product family.<\/p>\n<p class=\"srx-c-gatenote\">Full PDF documents are available after a free sign-in. Public summaries remain available below.<\/p>\n<\/div>\n<div aria-live=\"polite\" class=\"srx-c-count\"><strong id=\"sct-visible-count\">11<\/strong><span>shown<\/span><\/div>\n<\/div>\n<div class=\"srx-c-controls\">\n<label class=\"sct-search\" for=\"sct-search-input\">Search documents<\/label>\n<div class=\"srx-c-searchwrap\">\n<svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-search\"><\/use><\/svg>\n<input autocomplete=\"off\" id=\"sct-search-input\" placeholder=\"Search FDA, ANVISA, ISO 13485, Canada, Intertek...\" type=\"search\"\/>\n<\/div>\n<div aria-label=\"Certificate categories\" class=\"sct-filters\">\n<button aria-pressed=\"true\" class=\"is-active\" data-filter=\"all\" type=\"button\">All<\/button>\n<button aria-pressed=\"false\" data-filter=\"regulatory\" type=\"button\">Regulatory Registrations<\/button>\n<button aria-pressed=\"false\" data-filter=\"eu\" type=\"button\">EU \/ CE &amp; MDR<\/button>\n<button aria-pressed=\"false\" data-filter=\"quality\" type=\"button\">Quality &amp; Safety<\/button>\n<button aria-pressed=\"false\" data-filter=\"global\" type=\"button\">Global \/ IP Documentation<\/button>\n<\/div>\n<label class=\"srx-cert-series-label\" for=\"sct-series-filter\">Product family<\/label><select id=\"sct-series-filter\"><option value=\"all\">All product families<\/option><option value=\"d\">D Series<\/option><option value=\"l\">L Series<\/option><option value=\"c\">C Series<\/option><\/select><\/div>\n<p class=\"srx-c-note\"><span class=\"srx-med srx-med--sm srx-med--amber\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-bolt\"><\/use><\/svg><\/span><span class=\"srx-c-notetext\">Document dates refer to the supplied records. The library update date records when the files on this page were replaced.<\/span><\/p>\n<div class=\"srx-c-lib\" id=\"sct-cert-grid\">\n<div aria-label=\"Regulatory Registrations\" class=\"srx-c-group\" role=\"group\">\n<div class=\"srx-c-grouphead\">\n<span class=\"srx-med srx-med--sm\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-award\"><\/use><\/svg><\/span>\n<span class=\"srx-eyebrow\">Regulatory Registrations<\/span>\n<span class=\"srx-c-groupline\"><\/span>\n<\/div>\n<div class=\"srx-c-grid\">\n<article class=\"sct-cert-card\" data-category=\"regulatory\" data-search=\"suresult australia tga artg 360011 public summary therapeutic goods administration artg 360011 d series l series c series\" data-series=\"d l c\" id=\"tga-artg\">\n<div class=\"srx-c-chips\" data-index=\"01\"><span class=\"srx-c-region\">Australia<\/span><span class=\"srx-c-type\">Public summary<\/span><\/div>\n<div class=\"srx-c-logo\"><img alt=\"Therapeutic Goods Administration logo\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/www.tga.gov.au\/sites\/default\/files\/2025-05\/DHAC-TGA-strip-logo-black-730x151.png\"\/><\/div>\n<h3>Suresult Australia TGA ARTG 360011 Public Summary<\/h3>\n<p>Public summary for ARTG entry 360011, including the Australian sponsor, device classification and intended purpose. The supplied record names the portable wireless ultrasound system in the D, L and C series.<\/p>\n<dl class=\"srx-cert-facts\"><dt>Body \/ source<\/dt><dd>Therapeutic Goods Administration<\/dd><dt>Product family<\/dt><dd>D Series, L Series, C Series<\/dd><dt>Document date<\/dt><dd>25 August 2026 (summary produced)<\/dd><\/dl><a aria-label=\"View Public Summary: Suresult Australia TGA ARTG 360011 Public Summary\" class=\"srx-c-btn\" href=\"https:\/\/suresultmed.com\/cert-download\/tga-artg\/\" rel=\"noopener\" target=\"_blank\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-doc\"><\/use><\/svg>View Public Summary<\/a>\n<\/article>\n<article class=\"sct-cert-card\" data-category=\"regulatory\" data-search=\"suresult fda 510(k) wireless ultrasound documentation u.s. food and drug administration 510(k) correspondence; iyn \/ iyo \/ itx d series l series c series\" data-series=\"d l c\" id=\"fda-510k\">\n<div class=\"srx-c-chips\" data-index=\"02\"><span class=\"srx-c-region\">United States<\/span><span class=\"srx-c-type\">Regulatory document<\/span><\/div>\n<div class=\"srx-c-logo\"><img alt=\"FDA logo\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/suresultmed.com\/wp-content\/uploads\/2025\/02\/fda-logo-icon.png\"\/><\/div>\n<h3>Suresult FDA 510(k) Wireless Ultrasound Documentation<\/h3>\n<p>FDA 510(k) correspondence concerning an ultrasonic pulsed Doppler imaging system. The supplied document identifies Class II and product codes IYN, IYO and ITX, and names the D, L and C series.<\/p>\n<dl class=\"srx-cert-facts\"><dt>Body \/ source<\/dt><dd>U.S. Food and Drug Administration<\/dd><dt>Product family<\/dt><dd>D Series, L Series, C Series<\/dd><dt>Document date<\/dt><dd>13 October 2022<\/dd><\/dl><a aria-label=\"View FDA Document: Suresult FDA 510(k) Wireless Ultrasound Documentation\" class=\"srx-c-btn\" href=\"https:\/\/suresultmed.com\/cert-download\/fda-510k\/\" rel=\"noopener\" target=\"_blank\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-doc\"><\/use><\/svg>View FDA Document<\/a>\n<\/article>\n<article class=\"sct-cert-card\" data-category=\"regulatory\" data-search=\"suresult brazil anvisa authorization reference suresult documentation system registro 81535520003; srs-anvisa-2026-0519 d series l series c series\" data-series=\"d l c\" id=\"anvisa-brazil\">\n<div class=\"srx-c-chips\" data-index=\"03\"><span class=\"srx-c-region\">Brazil \/ ANVISA<\/span><span class=\"srx-c-type\">Authorization reference<\/span><\/div>\n<div class=\"srx-c-logo\"><img alt=\"ANVISA logo\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/suresultmed.com\/wp-content\/uploads\/2025\/02\/anvisa.png\"\/><\/div>\n<h3>Suresult Brazil ANVISA Authorization Reference<\/h3>\n<p>Brazil-market documentation reference listing ANVISA Registro 81535520003 and process 25351.022590\/2020-24. This dedicated file covers the portable wireless ultrasound D, L and C series.<\/p>\n<dl class=\"srx-cert-facts\"><dt>Body \/ source<\/dt><dd>Suresult Documentation System<\/dd><dt>Product family<\/dt><dd>D Series, L Series, C Series<\/dd><dt>Document date<\/dt><dd>22 January 2025 (listed in document)<\/dd><\/dl><a aria-label=\"View ANVISA Reference: Suresult Brazil ANVISA Authorization Reference\" class=\"srx-c-btn\" href=\"https:\/\/suresultmed.com\/cert-download\/anvisa-brazil\/\" rel=\"noopener\" target=\"_blank\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-doc\"><\/use><\/svg>View ANVISA Reference<\/a>\n<\/article>\n<article class=\"sct-cert-card\" data-category=\"regulatory\" data-search=\"suresult health canada medical device licence 107656 health canada licence 107656 d series l series c series\" data-series=\"d l c\" id=\"health-canada\">\n<div class=\"srx-c-chips\" data-index=\"04\"><span class=\"srx-c-region\">Canada<\/span><span class=\"srx-c-type\">Device licence<\/span><\/div>\n<div class=\"srx-c-logo\"><img alt=\"Health Canada logo\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/3\/3f\/Health_Canada_logo.svg\"\/><\/div>\n<h3>Suresult Health Canada Medical Device Licence 107656<\/h3>\n<p>Medical Device Licence 107656 identifies a Class III device family. Its accompanying device list includes CPROBE types C, CL, CT and L; consult that list for the recorded device identifiers.<\/p>\n<dl class=\"srx-cert-facts\"><dt>Body \/ source<\/dt><dd>Health Canada<\/dd><dt>Product family<\/dt><dd>D Series, L Series, C Series<\/dd><dt>Document date<\/dt><dd>22 April 2022 (first issue)<\/dd><\/dl><a aria-label=\"View Device Licence: Suresult Health Canada Medical Device Licence 107656\" class=\"srx-c-btn\" href=\"https:\/\/suresultmed.com\/cert-download\/health-canada\/\" rel=\"noopener\" target=\"_blank\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-doc\"><\/use><\/svg>View Device Licence<\/a>\n<\/article>\n<\/div>\n<\/div>\n<div aria-label=\"EU \/ CE &amp; MDR\" class=\"srx-c-group\" role=\"group\">\n<div class=\"srx-c-grouphead\">\n<span class=\"srx-med srx-med--sm\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-check\"><\/use><\/svg><\/span>\n<span class=\"srx-eyebrow\">EU \/ CE &amp; MDR<\/span>\n<span class=\"srx-c-groupline\"><\/span>\n<\/div>\n<div class=\"srx-c-grid\">\n<article class=\"sct-cert-card\" data-category=\"eu\" data-search=\"suresult eu mdr qms certificate | intertek nb 2862 intertek medical notified body ab 26970392216212; nb 2862 d series l series c series\" data-series=\"d l c\" id=\"eu-mdr-qms\">\n<div class=\"srx-c-chips\" data-index=\"05\"><span class=\"srx-c-region\">EU \/ MDR<\/span><span class=\"srx-c-type\">QMS certificate<\/span><\/div>\n<div class=\"srx-c-logo\"><img alt=\"Intertek logo\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/cdn.intertek.com\/intranet-intertek-com\/images\/global\/roundel-favicon-x.png\"\/><\/div>\n<h3>Suresult EU MDR QMS Certificate | Intertek NB 2862<\/h3>\n<p>EU Quality Management System certificate referencing Regulation (EU) 2017\/745, Annex IX Chapters I and III. The supplied certificate identifies Intertek NB 2862 and the portable wireless ultrasound D, L and C series.<\/p>\n<dl class=\"srx-cert-facts\"><dt>Body \/ source<\/dt><dd>Intertek Medical Notified Body AB<\/dd><dt>Product family<\/dt><dd>D Series, L Series, C Series<\/dd><dt>Document date<\/dt><dd>22 January 2025<\/dd><\/dl><a aria-label=\"View QMS Certificate: Suresult EU MDR QMS Certificate | Intertek NB 2862\" class=\"srx-c-btn\" href=\"https:\/\/suresultmed.com\/cert-download\/eu-mdr-qms\/\" rel=\"noopener\" target=\"_blank\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-doc\"><\/use><\/svg>View QMS Certificate<\/a>\n<\/article>\n<article class=\"sct-cert-card\" data-category=\"eu\" data-search=\"suresult eu declaration of conformity | d, l &amp; c series suresult industrial co., ltd. (declarant) ss-ctf-pl01-01-01, ver. a\/1 d series l series c series\" data-series=\"d l c\" id=\"eu-doc\">\n<div class=\"srx-c-chips\" data-index=\"06\"><span class=\"srx-c-region\">EU \/ CE<\/span><span class=\"srx-c-type\">Declaration<\/span><\/div>\n<div class=\"srx-c-logo\"><img alt=\"CE marking\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/suresultmed.com\/wp-content\/uploads\/2025\/02\/ce-logo-icon.webp\"\/><\/div>\n<h3>Suresult EU Declaration of Conformity | D, L &amp; C Series<\/h3>\n<p>Manufacturer declaration referencing Regulation (EU) 2017\/745 for the D, L and C series. The document includes classification, the conformity-assessment route, and a list of applicable standards, including biological evaluation and electrical safety references.<\/p>\n<dl class=\"srx-cert-facts\"><dt>Body \/ source<\/dt><dd>Suresult Industrial Co., Ltd. (declarant)<\/dd><dt>Product family<\/dt><dd>D Series, L Series, C Series<\/dd><dt>Document date<\/dt><dd>10 April 2025 (date stated)<\/dd><\/dl><a aria-label=\"View Declaration: Suresult EU Declaration of Conformity | D, L &amp; C Series\" class=\"srx-c-btn\" href=\"https:\/\/suresultmed.com\/cert-download\/eu-doc\/\" rel=\"noopener\" target=\"_blank\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-doc\"><\/use><\/svg>View Declaration<\/a>\n<\/article>\n\n<\/div>\n<\/div>\n<div aria-label=\"Quality &amp; Safety\" class=\"srx-c-group\" role=\"group\">\n<div class=\"srx-c-grouphead\">\n<span class=\"srx-med srx-med--sm\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-beaker\"><\/use><\/svg><\/span>\n<span class=\"srx-eyebrow\">Quality &amp; Safety<\/span>\n<span class=\"srx-c-groupline\"><\/span>\n<\/div>\n<div class=\"srx-c-grid\">\n<article class=\"sct-cert-card\" data-category=\"quality\" data-search=\"suresult iso 13485:2016 medical device qms certificate intertek 0096442-01; iso 13485:2016 d series l series c series\" data-series=\"d l c\" id=\"iso-13485\">\n<div class=\"srx-c-chips\" data-index=\"07\"><span class=\"srx-c-region\">Quality System<\/span><span class=\"srx-c-type\">QMS certificate<\/span><\/div>\n<div class=\"srx-c-logo\"><img alt=\"ISO logo\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/e\/e3\/ISO_Logo_%28Red_square%29.svg\"\/><\/div>\n<h3>Suresult ISO 13485:2016 Medical Device QMS Certificate<\/h3>\n<p>ISO 13485:2016 quality management system certificate. The stated scope covers design, manufacture and servicing of diagnostic ultrasound systems and the portable wireless ultrasound D, L and C series.<\/p>\n<dl class=\"srx-cert-facts\"><dt>Body \/ source<\/dt><dd>Intertek<\/dd><dt>Product family<\/dt><dd>D Series, L Series, C Series<\/dd><dt>Document date<\/dt><dd>18 November 2022<\/dd><\/dl><a aria-label=\"View ISO Certificate: Suresult ISO 13485:2016 Medical Device QMS Certificate\" class=\"srx-c-btn\" href=\"https:\/\/suresultmed.com\/cert-download\/iso-13485\/\" rel=\"noopener\" target=\"_blank\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-doc\"><\/use><\/svg>View ISO Certificate<\/a>\n<\/article>\n\n<article class=\"sct-cert-card\" data-category=\"quality\" data-search=\"suresult iec 60601-1 safety evidence &amp; mdr technical summary technical documentation reviewer (as stated) mdr-60601-tr-2026-0519 d series l series c series\" data-series=\"d l c\" id=\"iec-60601-1\">\n<div class=\"srx-c-chips\" data-index=\"08\"><span class=\"srx-c-region\">Safety Evidence<\/span><span class=\"srx-c-type\">Technical summary<\/span><\/div>\n<div class=\"srx-c-logo\"><img alt=\"IEC logo\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/3\/3e\/International_Electrotechnical_Commission_Logo.svg\"\/><\/div>\n<h3>Suresult IEC 60601-1 Safety Evidence &amp; MDR Technical Summary<\/h3>\n<p>Document-based technical review summary referencing IEC 60601-1 and EU MDR. It organizes electrical safety, essential performance, risk-management and software\/usability evidence for the D, L and C series.<\/p>\n<dl class=\"srx-cert-facts\"><dt>Body \/ source<\/dt><dd>Technical Documentation Reviewer (as stated)<\/dd><dt>Product family<\/dt><dd>D Series, L Series, C Series<\/dd><dt>Document date<\/dt><dd>19 May 2026<\/dd><\/dl><a aria-label=\"View Technical Summary: Suresult IEC 60601-1 Safety Evidence &amp; MDR Technical Summary\" class=\"srx-c-btn\" href=\"https:\/\/suresultmed.com\/cert-download\/iec-60601-1\/\" rel=\"noopener\" target=\"_blank\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-doc\"><\/use><\/svg>View Technical Summary<\/a>\n<\/article>\n<article class=\"sct-cert-card\" data-category=\"quality\" data-search=\"suresult mdsap &amp; sds \/ msds documentation summary quality and material compliance reviewer (as stated) srs-mdsap-msds-2026-0519 d series l series c series\" data-series=\"d l c\" id=\"mdsap-sds-msds\">\n<div class=\"srx-c-chips\" data-index=\"09\"><span class=\"srx-c-region\">Safety Docs<\/span><span class=\"srx-c-type\">Documentation summary<\/span><\/div>\n<div class=\"srx-c-logo\"><span class=\"srx-c-mark\">SDS<\/span><\/div>\n<h3>Suresult MDSAP &amp; SDS \/ MSDS Documentation Summary<\/h3>\n<p>Summary of quality-system and material-safety documentation for the D, L and C series. It describes MDSAP framework mapping, ISO 13485 links, supplier records and SDS\/MSDS file controls.<\/p>\n<dl class=\"srx-cert-facts\"><dt>Body \/ source<\/dt><dd>Quality and Material Compliance Reviewer (as stated)<\/dd><dt>Product family<\/dt><dd>D Series, L Series, C Series<\/dd><dt>Document date<\/dt><dd>19 May 2026<\/dd><\/dl><a aria-label=\"View Documentation Summary: Suresult MDSAP &amp; SDS \/ MSDS Documentation Summary\" class=\"srx-c-btn\" href=\"https:\/\/suresultmed.com\/cert-download\/mdsap-sds-msds\/\" rel=\"noopener\" target=\"_blank\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-doc\"><\/use><\/svg>View Documentation Summary<\/a>\n<\/article>\n<\/div>\n<\/div>\n<div aria-label=\"Global \/ IP Documentation\" class=\"srx-c-group\" role=\"group\">\n<div class=\"srx-c-grouphead\">\n<span class=\"srx-med srx-med--sm\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-globe\"><\/use><\/svg><\/span>\n<span class=\"srx-eyebrow\">Global \/ IP Documentation<\/span>\n<span class=\"srx-c-groupline\"><\/span>\n<\/div>\n<div class=\"srx-c-grid\">\n<article class=\"sct-cert-card\" data-category=\"global\" data-search=\"suresult global medical device authorizations summary global regulatory documentation reviewer (as stated) srs-gma-2026-0519 d series l series c series\" data-series=\"d l c\" id=\"global-summary\">\n<div class=\"srx-c-chips\" data-index=\"10\"><span class=\"srx-c-region\">Global<\/span><span class=\"srx-c-type\">Market documentation summary<\/span><\/div>\n<div class=\"srx-c-logo\"><span class=\"srx-c-mark\">GLO<\/span><\/div>\n<h3>Suresult Global Medical Device Authorizations Summary<\/h3>\n<p>International market-documentation summary for the D, L and C series. It organizes country-level records, labeling and instructions for use, representative information and post-market documentation by market.<\/p>\n<dl class=\"srx-cert-facts\"><dt>Body \/ source<\/dt><dd>Global Regulatory Documentation Reviewer (as stated)<\/dd><dt>Product family<\/dt><dd>D Series, L Series, C Series<\/dd><dt>Document date<\/dt><dd>19 May 2026<\/dd><\/dl><a aria-label=\"View Market Summary: Suresult Global Medical Device Authorizations Summary\" class=\"srx-c-btn\" href=\"https:\/\/suresultmed.com\/cert-download\/global-summary\/\" rel=\"noopener\" target=\"_blank\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-doc\"><\/use><\/svg>View Market Summary<\/a>\n<\/article>\n<article class=\"sct-cert-card\" data-category=\"global\" data-search=\"suresult euipo intellectual property documentation summary intellectual property documentation reviewer (as stated) srs-euipo-ip-2026-0519 d series l series c series\" data-series=\"d l c\" id=\"euipo-ip\">\n<div class=\"srx-c-chips\" data-index=\"11\"><span class=\"srx-c-region\">IP \/ EUIPO<\/span><span class=\"srx-c-type\">IP documentation summary<\/span><\/div>\n<div class=\"srx-c-logo\"><img alt=\"EUIPO logo\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/a.storyblok.com\/f\/139646\/417x114\/95f9a66f6f\/euipo-logo.png\/m\/640x0\/smart\/filters:quality(75)\"\/><\/div>\n<h3>Suresult EUIPO Intellectual Property Documentation Summary<\/h3>\n<p>European intellectual-property documentation summary for the D, L and C series. It organizes brand and design records, technical dossiers, product-family references and portfolio maintenance information.<\/p>\n<dl class=\"srx-cert-facts\"><dt>Body \/ source<\/dt><dd>Intellectual Property Documentation Reviewer (as stated)<\/dd><dt>Product family<\/dt><dd>D Series, L Series, C Series<\/dd><dt>Document date<\/dt><dd>19 May 2026<\/dd><\/dl><a aria-label=\"View IP Summary: Suresult EUIPO Intellectual Property Documentation Summary\" class=\"srx-c-btn\" href=\"https:\/\/suresultmed.com\/cert-download\/euipo-ip\/\" rel=\"noopener\" target=\"_blank\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-doc\"><\/use><\/svg>View IP Summary<\/a>\n<\/article>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"srx-c-empty\" hidden=\"\" id=\"sct-empty-state\">No matching documents found. Clear the search or choose All.<\/div>\n<\/section>\n<!-- 3. DARK CLOSING BAND -->\n<section aria-labelledby=\"srx-cert-faq-title\" class=\"srx-c-sec srx-cert-faq\"><h2 id=\"srx-cert-faq-title\">Questions About Suresult Documentation<\/h2><details><summary>Which ultrasound models are listed?<\/summary><p>The supplied documents name the D, L and C series. Check the model and device-identifier list within the relevant PDF when matching a specific probe to a record.<\/p><\/details><details><summary>How is an EU declaration different from a QMS certificate?<\/summary><p>The declaration states the manufacturer&#8217;s conformity position for the listed device family. A QMS certificate describes the assessed quality management system and its scope. Both document types are identified separately above.<\/p><\/details><details><summary>Where can I find the Brazil ANVISA reference?<\/summary><p>The Brazil ANVISA entry now opens its own dedicated reference PDF, separate from the Global Medical Device Authorizations Summary.<\/p><\/details><details><summary>How do I download a document?<\/summary><p>Select the document button, then sign in or create a free account. After sign-in, the requested PDF opens for review.<\/p><\/details><\/section><section class=\"srx-c-sec srx-c-close\">\n<span class=\"srx-med srx-med--seal srx-med--dark\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-seal\"><\/use><\/svg><\/span>\n<div class=\"srx-eyebrow\">Document library<\/div>\n<h2>Which Documents Should You Review?<\/h2>\n<p class=\"srx-c-deck\">Start with the relevant market record and its product scope. The EU Declaration of Conformity describes the manufacturer declaration; QMS certificates describe quality-system scope. Technical and market summaries organize supporting evidence and should be read alongside the underlying documents.<\/p>\n<p class=\"srx-c-contact\"><a class=\"srx-pill\" href=\"mailto:info@suresultmed.com\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-mail\"><\/use><\/svg>info@suresultmed.com<\/a><a class=\"srx-pill\" href=\"tel:+17477776278\"><svg aria-hidden=\"true\" class=\"srx-i\"><use href=\"#c-phone\"><\/use><\/svg>+1 747 777 6278<\/a><\/p>\n<\/section>\n<\/div>\n<script>(function(){\nconst root=document.getElementById('suresult-certifications-trust-center');\nif(!root||root.dataset.ready==='true')return;root.dataset.ready='true';\nconst cards=Array.from(root.querySelectorAll('.sct-cert-card'));\nconst search=root.querySelector('#sct-search-input'),series=root.querySelector('#sct-series-filter');\nconst buttons=Array.from(root.querySelectorAll('.sct-filters button'));\nconst count=root.querySelector('#sct-visible-count'),empty=root.querySelector('#sct-empty-state');\nlet category='all';\nconst normalize=v=>String(v||'').toLowerCase().replace(\/[^a-z0-9]+\/g,' ').trim();\nfunction apply(){let shown=0;const words=normalize(search.value).split(' ').filter(Boolean);\ncards.forEach(card=>{const hay=normalize(card.textContent+' '+card.dataset.search);\ncard.hidden=!((category==='all'||card.dataset.category===category)&&(series.value==='all'||card.dataset.series.split(' ').includes(series.value))&&words.every(w=>hay.includes(w)));if(!card.hidden)shown++;});\nroot.querySelectorAll('.srx-c-group').forEach(g=>{g.hidden=!Array.from(g.querySelectorAll('.sct-cert-card')).some(c=>!c.hidden);});\ncount.textContent=String(shown);empty.hidden=shown!==0;}\nbuttons.forEach(b=>b.addEventListener('click',()=>{category=b.dataset.filter;buttons.forEach(x=>{x.classList.toggle('is-active',x===b);x.setAttribute('aria-pressed',String(x===b));});apply();}));\nsearch.addEventListener('input',apply);series.addEventListener('change',apply);apply();\n})();<\/script>\n\n<script id=\"srx-certificate-schema\" type=\"application\/ld+json\">{\"@context\": \"https:\/\/schema.org\", \"@graph\": [{\"@type\": \"CollectionPage\", \"@id\": \"https:\/\/suresultmed.com\/certifications-compliance\/#certificate-collection\", \"url\": \"https:\/\/suresultmed.com\/certifications-compliance\/\", \"name\": \"Suresult Ultrasound Certifications & Regulatory Documents\", \"dateModified\": \"2026-09-05\", \"mainEntity\": {\"@id\": \"https:\/\/suresultmed.com\/certifications-compliance\/#document-library\"}}, {\"@type\": \"ItemList\", \"@id\": \"https:\/\/suresultmed.com\/certifications-compliance\/#document-library\", \"numberOfItems\": 11, \"itemListElement\": [{\"@type\": \"ListItem\", \"position\": 1, \"item\": {\"@type\": \"DigitalDocument\", \"@id\": \"https:\/\/suresultmed.com\/certifications-compliance\/#tga-artg\", \"url\": \"https:\/\/suresultmed.com\/certifications-compliance\/#tga-artg\", \"name\": \"Suresult Australia TGA ARTG 360011 Public Summary\", \"description\": \"Public summary for ARTG entry 360011, including the Australian sponsor, device classification and intended purpose. 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