{"id":3982,"date":"2025-06-10T23:46:37","date_gmt":"2025-06-10T23:46:37","guid":{"rendered":"https:\/\/veraqueconsulting.com\/mx\/?p=3982"},"modified":"2025-06-10T23:46:37","modified_gmt":"2025-06-10T23:46:37","slug":"medical-device-sterilization-and-regulatory-requirements-for-registration-in-mexico","status":"publish","type":"post","link":"https:\/\/veraqueconsulting.com\/mx\/medical-device-sterilization-and-regulatory-requirements-for-registration-in-mexico\/","title":{"rendered":"Medical Device Sterilization and Regulatory Requirements for Registration in Mexico\u00a0"},"content":{"rendered":"<p class=\"ai-optimize-8 ai-optimize-introduction\"><span data-contrast=\"auto\">Medical devices that are in contact with human tissues represent a significant risk of infection and cross-contamination if not properly sterilized. Ensuring sterility for single-use, reusable, or ready-to-sterilize devices is critical for patient safety and regulatory compliance. <\/span><\/p>\n<p>&nbsp;<\/p>\n<p class=\"ai-optimize-8 ai-optimize-introduction\"><span data-contrast=\"auto\">Manufacturers must evaluate sterilization methods during the development phase to meet international and local standards. This guide provides an overview of sterilization methods, applicable <\/span><a href=\"https:\/\/veraqueconsulting.com\/mx\/applicable-standards-for-medical-devices\/\" target=\"_blank\" rel=\"noopener\"><span data-contrast=\"none\">international<\/span><\/a><span data-contrast=\"auto\"> standards, and key regulatory requirements for <\/span><a href=\"https:\/\/veraqueconsulting.com\/mx\/ultimate-guide-for-regulatory-affairs-in-mexico\/#routes\" target=\"_blank\" rel=\"noopener\"><span data-contrast=\"none\">registering<\/span><\/a><span data-contrast=\"auto\"> sterile medical devices in Mexico.\u00a0\u00a0<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-9\"><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<h3 class=\"ai-optimize-10\"><b><span data-contrast=\"auto\">Sterilization Methods\u00a0<\/span><\/b><span data-ccp-props=\"{}\">\u00a0<\/span><\/h3>\n<p class=\"ai-optimize-11\"><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-12\"><span data-contrast=\"auto\">Sterilization of medical devices is an essential step to eliminate microbial contamination and ensure device safety. The most common methods include:\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<ul>\n<li class=\"ai-optimize-13\" data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\"><b><span data-contrast=\"auto\">Moist Heat (Steam)<\/span><\/b><span data-contrast=\"auto\">: Effective for heat-resistant materials, widely used in autoclaving.\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/li>\n<\/ul>\n<ul>\n<li class=\"ai-optimize-14\" data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\"><b><span data-contrast=\"auto\">Dry Heat<\/span><\/b><span data-contrast=\"auto\">: Suitable for moisture-sensitive devices.\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/li>\n<\/ul>\n<ul>\n<li class=\"ai-optimize-15\" data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\"><b><span data-contrast=\"auto\">Radiation (Gamma, E-Beam)<\/span><\/b><span data-contrast=\"auto\">: Penetrates packaging, ideal for single-use devices like syringes and catheters.\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/li>\n<\/ul>\n<ul>\n<li class=\"ai-optimize-16\" data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\"><b><span data-contrast=\"auto\">Ethylene Oxide (EtO)<\/span><\/b><span data-contrast=\"auto\">: A low-temperature gas sterilization method, particularly useful for polymers, multi-layer packaging, and complex devices (e.g., catheters, <\/span><a href=\"https:\/\/veraqueconsulting.com\/mx\/classification-and-grouping-for-stents-in-mexico\/\" target=\"_blank\" rel=\"noopener\"><span data-contrast=\"none\">stents<\/span><\/a><span data-contrast=\"auto\">).\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/li>\n<\/ul>\n<ul>\n<li class=\"ai-optimize-17\" data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\"><b><span data-contrast=\"auto\">Vaporized Hydrogen Peroxide &amp; Chlorine Dioxide<\/span><\/b><span data-contrast=\"auto\">: Used for sensitive electronics and heat-labile materials.\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/li>\n<\/ul>\n<p class=\"ai-optimize-18\"><span data-ccp-props=\"{&quot;335559685&quot;:720}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-19\"><span data-ccp-props=\"{&quot;335559685&quot;:720}\">\u00a0<\/span><\/p>\n<h3 class=\"ai-optimize-20\"><b><span data-contrast=\"auto\">The critical role of EtO\u00a0<\/span><\/b><span data-ccp-props=\"{}\">\u00a0<\/span><\/h3>\n<p class=\"ai-optimize-21\"><span data-contrast=\"auto\">EtO sterilization is one of the most widely used methods due to its compatibility with a broad range of materials, including plastics, metals, and glass. However, manufacturers must validate residual limits in compliance with <\/span><a href=\"https:\/\/www.google.com\/url?sa=t&amp;rct=j&amp;q=&amp;esrc=s&amp;source=web&amp;cd=&amp;cad=rja&amp;uact=8&amp;ved=2ahUKEwjMnMG9muGNAxWy5MkDHQZtKPYQFnoECAkQAQ&amp;url=https%3A%2F%2Ftranslate.google.com%2Ftranslate%3Fu%3Dhttps%3A%2F%2Fwww.iso.org%2Fstandard%2F34213.html%26hl%3Des%26sl%3Den%26tl%3Des%26client%3Dsrp&amp;usg=AOvVaw1TFHlMfh8lWAlmbde9TRRg&amp;opi=89978449\" target=\"_blank\" rel=\"noopener\"><span data-contrast=\"none\">ISO 10993-7<\/span><\/a><span data-contrast=\"auto\"> to ensure patient safety.\u00a0<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-22\"><span data-contrast=\"auto\">\u00a0<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<h3 class=\"ai-optimize-23\"><b><span data-contrast=\"auto\">International Standards for Sterilization<\/span><\/b><span data-ccp-props=\"{}\">\u00a0<\/span><\/h3>\n<p class=\"ai-optimize-24\"><span data-contrast=\"auto\">To ensure sterility and regulatory compliance, manufacturers must adhere to internationally recognized standards, including:\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<ul>\n<li class=\"ai-optimize-25\" data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"2\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\"><b><span data-contrast=\"auto\">ISO 11135<\/span><\/b><span data-contrast=\"auto\">: Validation and routine control of EtO sterilization.\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/li>\n<\/ul>\n<ul>\n<li class=\"ai-optimize-26\" data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"2\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\"><b><span data-contrast=\"auto\">ISO 17665<\/span><\/b><span data-contrast=\"auto\">: Moist heat sterilization (e.g., autoclaving).\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/li>\n<\/ul>\n<ul>\n<li class=\"ai-optimize-27\" data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"2\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\"><b><span data-contrast=\"auto\">ISO 11137<\/span><\/b><span data-contrast=\"auto\">: Radiation sterilization.\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/li>\n<\/ul>\n<ul>\n<li class=\"ai-optimize-28\" data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"2\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\"><b><span data-contrast=\"auto\">ISO 11607<\/span><\/b><span data-contrast=\"auto\">: Packaging requirements for sterile medical devices.\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/li>\n<\/ul>\n<p class=\"ai-optimize-29\"><span data-ccp-props=\"{&quot;335559685&quot;:720}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-30\"><span data-contrast=\"auto\">And additionally:\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<ul>\n<li class=\"ai-optimize-31\" data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"2\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\"><a href=\"https:\/\/www.iso.org\/standard\/67943.html\" target=\"_blank\" rel=\"noopener\"><b><span data-contrast=\"none\">ISO 20417<\/span><\/b><\/a><b><span data-contrast=\"auto\"> &amp; ISO 15223-1<\/span><\/b><span data-contrast=\"auto\">: Standardized symbols and labeling (applicable items for sterile products).\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/li>\n<\/ul>\n<p class=\"ai-optimize-32\"><span data-ccp-props=\"{&quot;335559685&quot;:720}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-33\"><span data-contrast=\"auto\">Compliance with these standards streamlines submission for registration in Mexico<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-34\"><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<h3 class=\"ai-optimize-35\"><a href=\"https:\/\/www.gob.mx\/cms\/uploads\/attachment\/file\/876069\/GUIA_PARA_LA_OBTENCION_DEL_REGISTRO_SANITARIO_DE_DISPOSITIVOS_MEDICOS_CLASE_I-II-III_Y_SOFTWARE_COMO_DISPOSITIVO_MEDICO.pdf\" target=\"_blank\" rel=\"noopener\"><b><span data-contrast=\"none\">COFEPRIS Requirements<\/span><\/b><\/a><b><span data-contrast=\"auto\"> for Sterile Medical Devices<\/span><\/b><span data-ccp-props=\"{}\">\u00a0<\/span><\/h3>\n<p class=\"ai-optimize-36\"><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-37\"><span data-contrast=\"auto\">To obtain sanitary registration in Mexico, MHA must submit detailed documentation on sterilization processes, including:\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-38\"><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<ol>\n<li class=\"ai-optimize-39\">\n<h5 class=\"ai-optimize-59\"><b><span data-contrast=\"auto\"> Sterilization Process Overview\u00a0\u00a0<\/span><\/b><\/h5>\n<\/li>\n<\/ol>\n<p class=\"ai-optimize-40\"><span data-contrast=\"auto\">\u00a0\u00a0 &#8211; Description of the method (e.g., EtO, gamma radiation).\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-41\"><span data-contrast=\"auto\">\u00a0\u00a0 &#8211; Validation summary confirming a Sterility Assurance Level (SAL) of 10\u207b\u2076.\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p>&nbsp;<\/p>\n<ol start=\"2\">\n<li class=\"ai-optimize-42\">\n<h5 class=\"ai-optimize-60\"><b><span data-contrast=\"auto\"> Sterility Report &amp; Certificate\u00a0\u00a0<\/span><\/b><\/h5>\n<\/li>\n<\/ol>\n<p class=\"ai-optimize-43\"><span data-contrast=\"auto\">\u00a0\u00a0 &#8211; Microbiological test results, certified by the responsible evaluator.\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-44\"><span data-contrast=\"auto\">\u00a0\u00a0 &#8211; For EtO sterilization, residual testing reports (ethylene oxide and ethylene chlorohydrin levels).\u00a0<\/span><\/p>\n<p class=\"ai-optimize-44\"><span data-contrast=\"auto\">\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<ol start=\"3\">\n<li class=\"ai-optimize-45\">\n<h5 class=\"ai-optimize-61\"><b><span data-contrast=\"auto\"> Reusable Device Requirements\u00a0\u00a0<\/span><\/b><\/h5>\n<\/li>\n<\/ol>\n<p class=\"ai-optimize-46\"><span data-contrast=\"auto\">\u00a0\u00a0 &#8211; Evidence that the device maintains its performance after repeated sterilization cycles.\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-47\"><span data-contrast=\"auto\">\u00a0\u00a0 &#8211; Clear instructions on re-sterilization methodology and maximum allowable cycles.\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p>&nbsp;<\/p>\n<ol start=\"4\">\n<li class=\"ai-optimize-48\">\n<h5 class=\"ai-optimize-63\"><a href=\"https:\/\/veraqueconsulting.com\/mx\/label-and-registration-designs\/\" target=\"_blank\" rel=\"noopener\"><b><span data-contrast=\"none\">Labeling<\/span><\/b><\/a><b><span data-contrast=\"auto\"> &amp; <\/span><\/b><a href=\"https:\/\/veraqueconsulting.com\/mx\/instructions-for-use-and-user-manuals-for-medical-devices-in-mexico\/\" target=\"_blank\" rel=\"noopener\"><b><span data-contrast=\"none\">Instructions for Use<\/span><\/b><\/a><b><span data-contrast=\"auto\"> (IFU)\u00a0\u00a0<\/span><\/b><\/h5>\n<\/li>\n<\/ol>\n<p class=\"ai-optimize-49\"><span data-contrast=\"auto\"><br \/>\n&#8211; <\/span><a href=\"https:\/\/www.dof.gob.mx\/normasOficiales\/3570\/SALUD13_C\/SALUD13_C.htm\" target=\"_blank\" rel=\"noopener\"><span data-contrast=\"none\">NOM-137-SSA1-2008<\/span><\/a><span data-contrast=\"auto\"> indicates that labels <\/span><a href=\"https:\/\/veraqueconsulting.com\/mx\/about-labeling-requirements-for-medical-devices-in-mexico\/\" target=\"_blank\" rel=\"noopener\"><span data-contrast=\"none\">requirements<\/span><\/a><span data-contrast=\"auto\"> must specify:\u00a0\u00a0<\/span><\/p>\n<p class=\"ai-optimize-49\"><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-50\"><span data-contrast=\"auto\">\u00a0\u00a0\u00a0\u00a0 &#8211; Sterilization method (e.g., &#8220;Sterilized with Ethylene Oxide&#8221;).\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-51\"><span data-contrast=\"auto\">\u00a0\u00a0\u00a0\u00a0 &#8211; Whether the product is single-use or reusable.\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-52\"><span data-contrast=\"auto\">\u00a0 \u00a0 \u00a0&#8211; IFUs must include sterilization\/reprocessing instructions (in Spanish).\u00a0 <\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-53\"><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-54\"><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<h3 class=\"ai-optimize-55\"><b><span data-contrast=\"auto\">Conclusion\u00a0<\/span><\/b><span data-ccp-props=\"{}\">\u00a0<\/span><\/h3>\n<p>&nbsp;<\/p>\n<p class=\"ai-optimize-56\"><span data-contrast=\"auto\">Sterilization is a critical factor in medical device safety and regulatory compliance. Manufacturers must carefully select and validate their sterilization methods while ensuring full adherence to and international standards and COFEPRIS requirements for registration in Mexico.\u00a0\u00a0<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-57\"><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p class=\"ai-optimize-58\"><span data-contrast=\"auto\">For expert guidance on sterilization validation, regulatory strategy, and local submissions, contact our team at <\/span><a href=\"mailto:contact@veraqueconsulting.com\"><span data-contrast=\"none\">contact@veraqueconsulting.com<\/span><\/a><span data-contrast=\"auto\"> to ensure a smooth path to market approval in Mexico.\u00a0\u00a0<\/span><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Medical devices that are in contact with human tissues represent a significant risk of infection and cross-contamination if not properly sterilized. Ensuring sterility for single-use, reusable, or ready-to-sterilize devices is critical for patient safety and regulatory compliance. &nbsp; Manufacturers must evaluate sterilization methods during the development phase to meet international and local standards. This guide [&hellip;]<\/p>\n","protected":false},"author":6,"featured_media":3983,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[390],"tags":[],"class_list":["post-3982","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-mexico"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v28.0 (Yoast SEO v28.0) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Medical Device Sterilization Regulatory Requirements - Veraque Mexico<\/title>\n<meta name=\"description\" content=\"Discover about sterilization methods, applicable international standards and COFEPRIS requirements for sterile medical devices in Mexico.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" 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