{"version":"1.0","provider_name":"Clinipower Finland Oy","provider_url":"https:\/\/www.clinipower.fi\/en\/","author_name":"Sylvia Syv\u00e4nen","author_url":"https:\/\/www.clinipower.fi\/en\/author\/sylvia\/","title":"When is CE marking mandatory for medical devices? - Clinipower Finland Oy","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"XmqOMBL8hl\"><a href=\"https:\/\/www.clinipower.fi\/en\/when-is-ce-marking-mandatory-for-medical-devices\/\">When is CE marking mandatory for medical devices?<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.clinipower.fi\/en\/when-is-ce-marking-mandatory-for-medical-devices\/embed\/#?secret=XmqOMBL8hl\" width=\"600\" height=\"338\" title=\"&#8220;When is CE marking mandatory for medical devices?&#8221; &#8212; Clinipower Finland Oy\" data-secret=\"XmqOMBL8hl\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script>\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n\/\/# sourceURL=https:\/\/www.clinipower.fi\/wp-includes\/js\/wp-embed.min.js\n<\/script>\n","thumbnail_url":"https:\/\/www.clinipower.fi\/wp-content\/uploads\/2025\/07\/eurooppalainen-laaketiede-teknologia-laboratorio-led.webp","thumbnail_width":1024,"thumbnail_height":768,"description":"When is CE marking mandatory for medical devices? CE marking is mandatory for all medical devices placed on the EU market that fall within the scope of the Medical Device Regulation (MDR). The marking demonstrates that the device meets safety and performance requirements. The only exceptions are custom-made devices and devices used in clinical investigations."}