{"id":6515,"date":"2026-05-22T11:14:13","date_gmt":"2026-05-22T05:44:13","guid":{"rendered":"https:\/\/operonstrategist.com\/?p=6515"},"modified":"2026-05-22T11:16:10","modified_gmt":"2026-05-22T05:46:10","slug":"unique-device-identification-udi-system","status":"publish","type":"post","link":"https:\/\/operonstrategist.com\/br-en\/unique-device-identification-udi-system\/","title":{"rendered":"UDI-Unique Device Identification System (Easily Comply Your Medical Device)"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-post\" data-elementor-id=\"6515\" class=\"elementor elementor-6515\" data-elementor-post-type=\"post\">\n\t\t\t\t<div class=\"elementor-element elementor-element-6a97ba67 e-flex e-con-boxed e-con e-parent\" data-id=\"6a97ba67\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t<div class=\"elementor-element elementor-element-3ea1b196 e-con-full e-flex e-con e-child\" data-id=\"3ea1b196\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-133cc3c0 elementor-widget elementor-widget-heading\" data-id=\"133cc3c0\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h1 class=\"elementor-heading-title elementor-size-default\">UDI - Unique Device Identification<\/h1>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5cd4c7fc elementor-widget elementor-widget-text-editor\" data-id=\"5cd4c7fc\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">Medical device regulations were implemented in the European Union in 2021 to make the medical device safer, more effective, and easy to trace in case something goes wrong. With the technological advancement, it was the main concern for the EU-MDR to trace those devices that either shows failure or adverse event as they risk the health of their users as well. Thus EU-MDR came up with the idea of giving different codes to different devices, known as Unique device identification (UDI), and storing them in a database to be used further.<\/span><\/p><p><span style=\"font-weight: 400;\">Everyone involved in the medical device industry is responsible, from the manufacturer to the regulatory authority. Everyone must understand that devices directly impact the course of treatment or diagnosis and, thus, must be safe to use.\u00a0 hence As <\/span><a href=\"https:\/\/operonstrategist.com\/services\/turnkey-project\/quality-management-system\/\"><span style=\"font-weight: 400;\">QMS certification consultants<\/span><\/a><span style=\"font-weight: 400;\">, we can help our clients to get UDI process compliances as per the latest regulations into your QMS.\u00a0 A slight error can result in serious health injuries, loss of life, or damage to organs.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-5c5f08d1 e-con-full e-flex e-con e-child\" data-id=\"5c5f08d1\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t<div class=\"elementor-element elementor-element-7b33c866 e-con-full e-flex e-con e-child\" data-id=\"7b33c866\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-38179a30 elementor-widget elementor-widget-heading\" data-id=\"38179a30\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h4 class=\"elementor-heading-title elementor-size-default\">Regulatory Excellence for Global Medical Device Markets<\/h4>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5d47dfd7 elementor-widget elementor-widget-wpforms\" data-id=\"5d47dfd7\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"wpforms.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"wpforms-container wpforms-container-full wpforms-render-modern\" id=\"wpforms-6203\"><form id=\"wpforms-form-6203\" class=\"wpforms-validate wpforms-form wpforms-ajax-form\" data-formid=\"6203\" method=\"post\" enctype=\"multipart\/form-data\" action=\"\/br-en\/wp-json\/wp\/v2\/posts\/6515\" data-token=\"2dd94d4717abcf1a93946f590b1d18de\" 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id=\"wpforms-submit-6203\" class=\"wpforms-submit\" data-alt-text=\"Sending...\" data-submit-text=\"Submit\" aria-live=\"assertive\" value=\"wpforms-submit\">Submit<\/button><img decoding=\"async\" src=\"https:\/\/operonstrategist.com\/wp-content\/plugins\/wpforms\/assets\/images\/submit-spin.svg\" class=\"wpforms-submit-spinner\" style=\"display: none;\" width=\"26\" height=\"26\" alt=\"Loading\"><\/div><\/form><\/div>  <!-- .wpforms-container -->\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-2d8d581b e-flex e-con-boxed e-con e-parent\" data-id=\"2d8d581b\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-241699aa elementor-widget elementor-widget-heading\" data-id=\"241699aa\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">What is UDI - Unique Device Identification?\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-49f93091 elementor-widget elementor-widget-text-editor\" data-id=\"49f93091\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">Unique Device Identification (UDI) is a series of numbers or alphabets created through identification and coding and accepted globally. UDI helps to assign specific identification to each medical device that is present in the market or is about to be marketed. It helps trace the devices, except for custom-made and investigational devices.\u00a0<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5de30a0 elementor-widget elementor-widget-heading\" data-id=\"5de30a0\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">What Comprises the UDI System: \n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-662cdd91 e-con-full e-flex e-con e-child\" data-id=\"662cdd91\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-2c10108 elementor-widget elementor-widget-text-editor\" data-id=\"2c10108\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">Unique Device Identifier (UDI) comprises two parts:\u00a0<\/span><\/p><ol><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Unique device identifier-device identifier (UDI-DI)\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Unique device identifier \u2013 Production identifier (UDI-PI)\u00a0<\/span><\/li><\/ol><table><tbody><tr><td><p><span style=\"font-weight: 400;\">Basic UDI- DI\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">UDI-PI\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">A UDI device identifier (UDI-DI) is specific to a device, and the manufacturer provides information access as per Part B of Annex VI.\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">A UDI production identifier (UDI-PI) is specific to the device\u2019s production and the packaged device (if applicable).\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">\u00a0<\/span><\/p><\/td><\/tr><tr><td><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">It is the main key to accessing the information related to the device in the EUDAMED database.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">It is referenced through relevant documents such as a free sale certificate, EU confirmation declaration, technical documentation, etc.\u00a0\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">It identifies the devices and connects them with the same intended purpose device, risk class, essential design, and manufacturing.\u00a0\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">It does not appear on any trade item and is separate from the label or packaging. MDGC 2018-1v3 is the guidance document on basic UDI.\u00a0<\/span><\/li><\/ul><p><span style=\"font-weight: 400;\">\u00a0<\/span><\/p><\/td><td><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">If a lot, serial number, software identification, or expiry date is present on the label, it shall be part of UDI-PI.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">\u00a0If the manufacturing date is also present, it need not be included in UDI-PI.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">If the manufacturing date is present alone, it shall come under UDI-PI.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Characteristics of UDI-PI, such as lot and serial number, need to be defined by the manufacturer.\u00a0<\/span><\/li><\/ul><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Serial number shall be included in UDI-PI for active implantable devices.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Serial numbers and lot numbers shall be included in UDI-PI for implantable devices.\u00a0<\/span><\/li><\/ul><\/td><\/tr><\/tbody><\/table><p><span style=\"font-weight: 400;\">No UDI-PI information can be present in the UDI database.\u00a0<\/span><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Place the UDI-ID on the device label or the packaging.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">UDI shall be stored by economic health operators, healthcare institutions, and professionals as per paragraphs 8 and 9 of the EU-MDR.\u00a0<\/span><\/li><\/ul><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Establish the UDI database, the electronic system for unique device identification, per Article 28 of EU-MDR.<\/span><\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-2189fed elementor-widget elementor-widget-heading\" data-id=\"2189fed\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Why Is a UDI Required?<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5823df6 elementor-widget elementor-widget-text-editor\" data-id=\"5823df6\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">The UDI system\u2019s primary regulatory purpose is to increase patient safety. The implementation of a fully standardized system improves traceability, which benefits stakeholders in the medical device industry such as manufacturers, regulatory bodies, healthcare providers, and patients.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-1e102c0 elementor-widget elementor-widget-heading\" data-id=\"1e102c0\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Benefits of a UDI System\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-a04016b elementor-widget elementor-widget-text-editor\" data-id=\"a04016b\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">Implementing a Unique Device Identification (UDI) System for Medical Devices Offers Several Benefits to Various Stakeholders in the Healthcare Industry. Here Are Some Key Advantages of a Udi System:<\/span><\/p><p><span style=\"font-weight: 400;\">\u2013 Enhanced patient safety through accurate identification and traceability of medical devices.<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2013 Improved medical device management by providing critical information for inventory control and resource allocation.<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2013 Facilitates regulatory compliance, meeting UDI requirements set by regulatory authorities.<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2013 Enables efficient post-market surveillance for monitoring device performance and detecting adverse events.<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2013 Streamlines product recalls and field corrective actions by enabling precise identification of affected devices.<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2013 Supports medical device innovation and research through standardized and reliable data collection.<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">\u2013 Promotes transparency, accountability, and quality assurance in the healthcare industry.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-d9701da elementor-widget elementor-widget-heading\" data-id=\"d9701da\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Unique Device Identification Appearance on the Label or Package: <\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-aef597b elementor-widget elementor-widget-text-editor\" data-id=\"aef597b\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">A UDI carrier (automated identification for data capture) AIDC or (human readable interpretation) HRI shall be present on the label, the device, or the packaging. If space is less, UDI carriers can be placed on the next higher packaging level.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">The UDI shall be present in plain text, which can be read easily by human eyes in HRI form along, with AIDC. AIDC is a technique in which the unique device identifier is present in a form that healthcare professionals can enter easily into an electronic record. If there is a space constraint, then only AIDC shall be present.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">For the device used outside the healthcare institution, such as a home care device, HRI shall be present in case of space constraints.\u00a0<\/span><\/li><\/ul><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">For devices of class I and IIa, which are single-use devices, UDI shall not be required to present on individual packaging; instead, it shall present on a higher level of packaging.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">If the device is not a healthcare facility, the UDI instead of higher packaging shall be present on the individual packaging.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">The device is exclusively for sale through retail; the UDI-PI in AIDC shall not be present on the sale packaging.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">If the UDI carrier is readable or scannable from the packaging, then the UDI carrier is not needed.\u00a0<\/span><\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-d9b0ecf elementor-widget elementor-widget-heading\" data-id=\"d9b0ecf\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">UDI Issuing Entities:\u202f \n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5f905fb elementor-widget elementor-widget-text-editor\" data-id=\"5f905fb\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">After the launch of the call for application at the end of 2018 and the implementation of Decision EU 2019\/939, four entities were issued to provide manufacturers with a list of UDIs to assign the medical device:\u00a0<br \/>UDI HRI and AIDC are basic formats issued by all four entities, but these entities will update the content regularly. <br \/><\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-b27421a elementor-widget elementor-widget-heading\" data-id=\"b27421a\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">UDI Storage Requirements:<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-91e90e6 elementor-widget elementor-widget-text-editor\" data-id=\"91e90e6\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">The health state members encourage and require the health facilities to store and maintain the UDI, and preference shall be given to AIDC type, other than class III implantable devices.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">If the device belongs to a class III implantable device, then AIDC shall be stored, which was supplied with the device.\u00a0<\/span><\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-958abbd elementor-widget elementor-widget-heading\" data-id=\"958abbd\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Unique Device Identification Database: <\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-d7c8458 elementor-widget elementor-widget-text-editor\" data-id=\"d7c8458\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">European Union Commission set up the data to collect, validate, process and make data available to the common public. It is designed to ensure the information stored is adequate and correct, allows multiple users to access it, upload the information automatically, and can be downloaded. It does not include any UDI-PI or confidential information related to devices.\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">\u202f<\/span><span style=\"font-weight: 400;\">The EU-MDR gives a brief about how Unique identification numbers shall be assigned to each device, how they shall be placed, where to place, how to store, format, etc., so that medical device professionals can follow those rules. With the set of rules, the regulatory body of Europe aims to make the traceability of medical devices easy. With the help of traceability and updated databases of failures or adverse events, regulatory bodies are trying to make medical devices as safe as possible for the intended population.\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">As a leading medical device regulatory consultant, <\/span><a href=\"https:\/\/operonstrategist.com\/\"><span style=\"font-weight: 400;\">Operon Strategist<\/span><\/a><span style=\"font-weight: 400;\"> offers comprehensive solutions tailored to your specific needs. From FDA submissions to CE marking and beyond, our experienced team will guide you every step of the way. Ensure compliance, accelerate your market access, and gain a competitive edge. Also, we provide medical device regulatory services like <\/span><a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/cdsco-registration\/\"><span style=\"font-weight: 400;\">CDSCO Registration<\/span><\/a><span style=\"font-weight: 400;\">, <\/span><a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/fda-510k\/\"><span style=\"font-weight: 400;\">FDA 510k<\/span><\/a><span style=\"font-weight: 400;\">, <\/span><a href=\"https:\/\/operonstrategist.com\/services\/turnkey-project\/quality-management-system\/iso-13485\/\"><span style=\"font-weight: 400;\">ISO 13485 Certification<\/span><\/a><span style=\"font-weight: 400;\">, etc. <\/span><a href=\"https:\/\/operonstrategist.com\/contact-us\/\"><span style=\"font-weight: 400;\">Contact Operon Strategist<\/span><\/a><span style=\"font-weight: 400;\"> today for a smooth path to regulatory success. Let\u2019s revolutionize healthcare together.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>UDI &#8211; Unique Device Identification Medical device regulations were implemented in the European Union in 2021 to make the medical device safer, more effective, and easy to trace in case something goes wrong. With the technological advancement, it was the main concern for the EU-MDR to trace those devices that either shows failure or adverse [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":6516,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[55],"tags":[],"class_list":["post-6515","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-regulatory"],"_links":{"self":[{"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/posts\/6515","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/comments?post=6515"}],"version-history":[{"count":0,"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/posts\/6515\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/media\/6516"}],"wp:attachment":[{"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/media?parent=6515"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/categories?post=6515"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/tags?post=6515"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}