{"id":3449,"date":"2025-03-11T18:29:19","date_gmt":"2025-03-11T18:29:19","guid":{"rendered":"https:\/\/www.gilero.com\/uncategorized\/medical-device-labeling\/"},"modified":"2026-09-01T16:02:29","modified_gmt":"2026-09-01T16:02:29","slug":"medical-device-labeling","status":"publish","type":"blog","link":"https:\/\/www.sanner-group.com\/insights\/blog\/medical-device-labeling\/","title":{"rendered":"Medical Device Labeling"},"content":{"rendered":"\n<section id=\"armstrong-block-editor-block_efb87270497df1e3066b824c5f0e5cbe\" class=\"armstrong-block armstrong-block-editor\" >\n    <div class=\"container-fluid\">\n        <div class=\"row\">\n            <div class=\"col-lg-12\">\n                                <p><!-- wp:heading --><\/p>\n<h2 class=\"wp-block-heading\">What Is Medical Device Labeling?<\/h2>\n<p><!-- \/wp:heading --><\/p>\n<p><!-- wp:paragraph --><\/p>\n<p>Medical device labeling refers to all of the information that is provided to the consumer with the device itself. This includes symbols, warnings, instructions, and control labels applied to the device or incorporated into the design by color coding, printing, machining, or molding.<\/p>\n<p><!-- \/wp:paragraph --><\/p>\n<p><!-- wp:paragraph {\"className\":\"reduce-bottom-margin\"} --><\/p>\n<p class=\"reduce-bottom-margin\">Medical device labeling also refers to<\/p>\n<p><!-- \/wp:paragraph --><\/p>\n<p><!-- wp:list --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\"><!-- wp:list-item --><\/p>\n<li>Information display on the device\u2019s user interface<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>Information printed on the device\u2019s packaging or point-of-sale displays<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>Documents provided with the device, including manuals and instructions<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- \/wp:list --><\/p>\n<p><!-- wp:paragraph --><\/p>\n<p>Medical device labeling is not just the label on the device, but rather any labels on the pouch, box, instructions for use, etc. The leading international standard for medical device quality systems, <a href=\"https:\/\/www.sanner-group.com\/insights\/blog\/guide-iso-13485-medical-device-manufacturers\/\">ISO 13485<\/a>, states that a label is any information related to identification, technical description, intended purpose, and proper use of the device.<\/p>\n<p><!-- \/wp:paragraph --><\/p>\n<p><!-- wp:heading --><\/p>\n<h2 class=\"wp-block-heading\">What Are Medical Device Labeling Requirements?<\/h2>\n<p><!-- \/wp:heading --><\/p>\n<p><!-- wp:paragraph --><\/p>\n<p>Medical devices companies that sell their products in the US must adhere to the FDA\u2019s strict medical device labeling requirements. The purpose of these regulations is to help keep medical device users safe. The requirements for labeling a particular medical device depend on what type of device it is and what level of risk is involved.<\/p>\n<p><!-- \/wp:paragraph --><\/p>\n<p><!-- wp:paragraph --><\/p>\n<p>All medical device labels must include the name and address of the manufacturer, packer or distributor, and directions for use. Beyond these general requirements, medical device companies must determine the intended use and risk classification of their device to pinpoint their specific requirements. The FDA has published detailed regulations in <a href=\"https:\/\/www.accessdata.fda.gov\/scripts\/cdrh\/cfdocs\/cfcfr\/CFRSearch.cfm?CFRPart=801\" target=\"_blank\" rel=\"noopener noreferrer\">21 CFR Part 801<\/a>. In addition, electromechanical medical devices have labeling requirements defined in IEC 60601-1 Clause 7. The usability of the labeling is addressed in IEC 62366. Canada\u2019s regulations can be found in <a href=\"http:\/\/laws-lois.justice.gc.ca\/eng\/regulations\/sor-98-282\/FullText.html\" target=\"_blank\" rel=\"noopener noreferrer\">Canadian Medical Device Regulations<\/a> clause 21. Refer to <a href=\"https:\/\/eur-lex.europa.eu\/LexUriServ\/LexUriServ.do?uri=CONSLEG:1993L0042:20071011:en:PDF\">Medical Device Directive<\/a> Annex 1, clause 13 for EU regulations.<\/p>\n<p><!-- \/wp:paragraph --><\/p>\n<p><!-- wp:heading --><\/p>\n<h2 class=\"wp-block-heading\">The Importance of Proper Medical Device Labeling<\/h2>\n<p><!-- \/wp:heading --><\/p>\n<p><!-- wp:paragraph --><\/p>\n<p>A medical device label is intended to educate users, namely patients or healthcare providers, on how a device should be used, what risks are involved, and how to safely operate and maintain the device. Given that many medical devices are used by the patient at home, not under supervision by a medical expert, it\u2019s critical that devices give accurate information about how to use and interpret the device to avoid injury, illness, or death.<\/p>\n<p><!-- \/wp:paragraph --><\/p>\n<p><!-- wp:paragraph --><\/p>\n<p>For instance, a prefilled syringe allowing a patient to administer a measured dose of medication at home could help treat or prevent a specific disease when used correctly. If used incorrectly, a number of adverse effects could occur, such as injury from improper handling of the needle or an incomplete dose of medication. Because of these scenarios, a thorough analysis of <a href=\"https:\/\/www.sanner-group.com\/insights\/blog\/importance-human-factors-medical-drug-delivery-devices\/\" target=\"_blank\" rel=\"noreferrer noopener\">human factors and usability testing<\/a> is necessary to ensure device labeling covers all bases.<\/p>\n<p><!-- \/wp:paragraph --><\/p>\n<p><!-- wp:heading --><\/p>\n<h2 class=\"wp-block-heading\">The Do\u2019s and Don\u2019ts of Medical Device Labeling<\/h2>\n<p><!-- \/wp:heading --><\/p>\n<p><!-- wp:paragraph --><\/p>\n<p>Given how lengthy and varied medical device labeling requirements can be, the process can be tricky for medical or pharmaceutical companies attempting to create this labeling. Tips for what to do and what to avoid are outlined below. Note that each jurisdiction has its own requirements, so be sure to check regulations for each country or region where you plan to commercialize the device.<\/p>\n<p><!-- \/wp:paragraph --><\/p>\n<p><!-- wp:heading --><\/p>\n<h2 class=\"wp-block-heading\">What to Do<\/h2>\n<p><!-- \/wp:heading --><\/p>\n<p><!-- wp:paragraph {\"className\":\"reduce-bottom-margin\"} --><\/p>\n<p class=\"reduce-bottom-margin\">When labeling medical devices, do:<\/p>\n<p><!-- \/wp:paragraph --><\/p>\n<p><!-- wp:list --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\"><!-- wp:list-item --><\/p>\n<li>Include labeling early on in your design planning<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>Identify the device by make, model number, date of manufacture, and batch or serial number<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>Provide contact information for the manufacturer and\/or the local representative or distributor<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>Include the intended use and indications for use and any contraindications or possible side effects<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>List the box contents, meaning everything supplied with the device<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>Include instructions for correct usage<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>Include any warnings or cautions resulting from the risk management process<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>Use appropriate symbols where possible in the labeling of the device<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>Select label materials that will remain legible for the life of the device and are compatible with cleaning and sterilization methods defined in the instructions for use<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>Have someone with <a href=\"https:\/\/www.sanner-group.com\/capabilities\/regulatory-services\/\">regulatory<\/a> knowledge review the labeling before submitting the device for clearance<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- \/wp:list --><\/p>\n<p><!-- wp:heading --><\/p>\n<h2 class=\"wp-block-heading\">What Not to Do<\/h2>\n<p><!-- \/wp:heading --><\/p>\n<p><!-- wp:paragraph {\"className\":\"reduce-bottom-margin\"} --><\/p>\n<p class=\"reduce-bottom-margin\">The following should be avoided on medical device labels:<\/p>\n<p><!-- \/wp:paragraph --><\/p>\n<p><!-- wp:list --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\"><!-- wp:list-item --><\/p>\n<li>Including any text which contradicts the intended use or describes or refers to an off label use<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>Including any marketing statements that are not supported by data<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>Using the certifying body (e.g. CSA, ETL, UL) artwork on the product label without written permission<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- wp:list-item --><\/p>\n<ul class=\"wp-block-list\">\n<li style=\"list-style-type: none;\">\n<ul class=\"wp-block-list\">\n<li>Making any labeling changes after the device has gained regulatory clearance<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!-- \/wp:list-item --><\/p>\n<p><!-- \/wp:list --><\/p>\n<p><!-- wp:paragraph --><\/p>\n<p><em>Learn more from Sanner in these posts: <\/em><a href=\"https:\/\/www.sanner-group.com\/insights\/blog\/how-to-prepare-a-510k-submission\/\" target=\"_blank\" rel=\"noreferrer noopener\"><em>FDA 510(k) Submission Process: An Introduction &amp; How-To Guide<\/em><\/a><em> and <\/em><a href=\"https:\/\/www.sanner-group.com\/insights\/blog\/combination-products-overview\/\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Combination Products: Definition &amp; Overview<\/em><\/a><em>.<\/em><\/p>\n<p><!-- \/wp:paragraph --><\/p>\n<p><!-- wp:paragraph --><\/p>\n<p>Sanner is a trusted partner for medical and drug delivery devices from start to finish. For more information about our <a href=\"https:\/\/www.sanner-group.com\/capabilities\/\">services and capabilities<\/a>, <a href=\"https:\/\/www.sanner-group.com\/contact\">contact us<\/a> today.<\/p>\n<p><!-- \/wp:paragraph --><\/p>\n            <\/div>\n        <\/div>\n    <\/div>\n<\/section>","protected":false},"featured_media":3253,"template":"","blog_category":[89],"class_list":["post-3449","blog","type-blog","status-publish","has-post-thumbnail","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Understanding Medical Device Labeling - Gilero<\/title>\n<meta name=\"description\" content=\"Optimize your medical device labeling with our comprehensive guide. 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