{"id":24192,"date":"2020-07-15T15:44:42","date_gmt":"2020-07-15T15:44:42","guid":{"rendered":"http:\/\/www.sac-oac.ca\/drupal\/post\/programme-daudit-unique-des-materiels-medicaux-paumm\/"},"modified":"2024-07-17T10:09:10","modified_gmt":"2024-07-17T14:09:10","slug":"programme-daudit-unique-des-materiels-medicaux-paumm","status":"publish","type":"post","link":"https:\/\/eventsdev.sac-oac.ca\/fr\/programme-daudit-unique-des-materiels-medicaux-paumm\/","title":{"rendered":"Programme d\u2019audit unique des mat\u00e9riels m\u00e9dicaux (PAUMM)"},"content":{"rendered":"<p><span class=\"black\">As of January 1, 2019, Health Canada requires all manufacturers of<\/span>&nbsp;<a href=\"https:\/\/mailchi.mp\/sac-oac\/sac-news-upcoming-regulatory-changes-to-medical-devices-in-canada?e=%5bUNIQID%5d#Class%20Devices\" target=\"_blank\" rel=\"noopener\">class II, III, and IV medical devices<\/a>&nbsp;<span class=\"black\">sold in Canada to follow the<\/span>&nbsp;<a href=\"https:\/\/mailchi.mp\/sac-oac\/sac-news-upcoming-regulatory-changes-to-medical-devices-in-canada?e=%5bUNIQID%5d\" target=\"_blank\" rel=\"noopener\">Medical Device Single Audit Program<\/a>&nbsp;<span class=\"black\">(MDSAP).&nbsp;<\/span><\/p>\n<p><span class=\"black\">SAC members have raised concerns regarding the impact of MDSAP on their patients and clients, including access to the Passy-Muir Speaking Valve. The Passy-Muir Valve is currently an unlicensed medical device in Canada.<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><span class=\"black\">Health Canada has suggested the following alternatives to the Passy-Muir Speaking Valve:&nbsp;<\/span><br \/>\n&nbsp;<\/p>\n<table cellpadding=\"0\" cellspacing=\"0\">\n<tbody>\n<tr>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\"><strong>Licence no.<\/strong><\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\"><strong>Licence name<\/strong><\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\"><strong>Device ID<\/strong><\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\"><strong>Device name<\/strong><\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\"><strong>Website<\/strong><\/span><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\">8607<\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\">Montgomery Speaking Valves<\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\">143673<\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\">Montgomery Speaking Valves<\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><a href=\"https:\/\/www.bosmed.com\/en\/airway-management\/montgomeryr-cannula-system\/montgomeryr-cannula-speaking-valves\/\" target=\"_blank\" rel=\"noopener\">https:\/\/www.bosmed.com\/en\/airway-management\/montgomeryr-cannula-system\/montgomeryr-cannula-speaking-valves\/<\/a><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\">1845<\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\">Shiley Phonate Speaking Valve<\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\">182822<\/span><\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p><span class=\"black\">182823<\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\">Shiley Phonate Speaking Valve<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><span class=\"black\">Shiley Phonate Speaking Valve (With Oxygen Port)<\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><a href=\"https:\/\/www.medtronic.com\/covidien\/en-us\/products\/tracheostomy\/shiley-speaking-valves.html\" target=\"_blank\" rel=\"noopener\">https:\/\/www.medtronic.com\/covidien\/en-us\/products\/tracheostomy\/shiley-speaking-valves.html<\/a><\/p>\n<\/td>\n<\/tr>\n<tr>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\">94766<\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\">TRACOE Phon Assist II Speaking Valves REF 655-S AND REF 655-T With Attachable Tracoe Humid Assist II REF 645<\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\">804032<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><span class=\"black\">1001469<\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><span class=\"black\">Tracoe Humid Assist II<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><span class=\"black\">Tracoe Phon Assist II Speaking Valves<\/span><\/p>\n<\/td>\n<td style=\"vertical-align:top\">\n<p><a href=\"https:\/\/www.bryanmedical.net\/products\/tracoe\/tracoe-product-catalog\" target=\"_blank\" rel=\"noopener\">https:\/\/www.bryanmedical.net\/products\/tracoe\/tracoe-product-catalog<\/a><\/p>\n<p>&nbsp;<\/p>\n<p><span class=\"black\">(page 34 to 38)<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span class=\"black\">Health Canada has a<\/span> <a href=\"https:\/\/www.canada.ca\/en\/health-canada\/services\/drugs-health-products\/special-access\/medical-devices.html\" target=\"_blank\" rel=\"noopener\">Special Access Program<\/a> <span class=\"black\">to allow for access to unlicensed medical devices (such as the Passy-Muir Valve) in specific circumstances.&nbsp;<\/span><\/p>\n<p><span class=\"black\">The Special Access Program considers requests from health care professionals for access to unlicensed medical devices for emergency use, or if conventional therapies have failed, are unavailable or are unsuitable. Although Health Canada may issue an authorization for a medical device through this program, a manufacturer is not obligated to sell this medical device for special access purposes.&nbsp;<\/span><\/p>\n<p><span class=\"black\">A special access application would need to outline the circumstances&nbsp;for which approved devices are unsuitable or unavailable. Each application is considered on a case-by-case basis, and a previous authorization does not necessarily mean that another authorization will be granted.<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><span class=\"black\">For additional information about the Special Access Program, please refer to Health Canada guidance:<\/span><\/p>\n<p><a href=\"https:\/\/www.canada.ca\/en\/health-canada\/services\/drugs-health-products\/special-access\/medical-devices\/guidance-health-care-professionals-special-access-custom-made.html\" target=\"_blank\" rel=\"noopener\">https:\/\/www.canada.ca\/en\/health-canada\/services\/drugs-health-products\/special-access\/medical-devices\/guidance-health-care-professionals-special-access-custom-made.html<\/a><\/p>\n<p>&nbsp;<\/p>\n<p><span class=\"black\">SAC members and associates are encouraged to contact<\/span> <a href=\"mailto:meredith@sac-oac.ca\">meredith@sac-oac.ca<\/a> <span class=\"black\">should they encounter difficulty accessing an unlicensed medical device through the Special Access Program.<\/span><\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>As of January 1, 2019, Health Canada requires all manufacturers of&nbsp;class II, III, and IV medical devices&nbsp;sold in Canada to follow the&nbsp;Medical Device Single Audit Program&nbsp;(MDSAP).&nbsp; SAC members have raised concerns regarding the impact of MDSAP on their patients and clients, including access to the Passy-Muir Speaking Valve. The Passy-Muir Valve is currently an unlicensed [&hellip;]<\/p>\n","protected":false},"author":13,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_genesis_hide_title":false,"_genesis_hide_breadcrumbs":false,"_genesis_hide_singular_image":false,"_genesis_hide_footer_widgets":false,"_genesis_custom_body_class":"","_genesis_custom_post_class":"","_genesis_layout":"","footnotes":""},"tags":[],"class_list":{"0":"post-24192","1":"post","2":"type-post","3":"status-publish","4":"format-standard","6":"category-nouvelles-doac","7":"entry"},"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Programme d\u2019audit unique des mat\u00e9riels m\u00e9dicaux (PAUMM) - SAC<\/title>\n<meta name=\"robots\" content=\"noindex, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Programme d\u2019audit unique des mat\u00e9riels m\u00e9dicaux (PAUMM) - SAC\" \/>\n<meta property=\"og:description\" content=\"As of January 1, 2019, Health Canada requires all manufacturers of&nbsp;class II, III, and IV medical devices&nbsp;sold in Canada to follow the&nbsp;Medical Device Single Audit Program&nbsp;(MDSAP).&nbsp; SAC members have raised concerns regarding the impact of MDSAP on their patients and clients, including access to the Passy-Muir Speaking Valve. 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