﻿<!-- edited with XMLSpy v2012 rel. 2 (x64) (http://www.altova.com) by Jeremy Morton (GS1 Sweden AB) -->
<codeList term="T4485" SDDversion="0" SDDupdated="2026-03-18" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:noNamespaceSchemaLocation="allcodes31.xsd">
	<urn>urn:gs1:gdd:cl:DeviceRiskClassMDD_AIMDD_IVDD</urn>
	<listName languageCode="en">Device risk class MDD/AIMDD/IVDD</listName>
	<listName languageCode="sv">Riskklass MDD/AIMDD/IVDD</listName>
	<GDDversion>3</GDDversion>
	<GDDupdated>2026-05-16</GDDupdated>
	<domain>shared</domain>
	<code>
    <value>AIMDD</value>
    <name languageCode="sv">Aktiva implantatbara medicintekniska produkter (AIMDD)</name>
    <name languageCode="en">Active Implantable Medical Devices (AIMDD)</name>
    <description languageCode="en">Class AIMDD for Medical Devices (according to EU Directive AIMDD 90/385/EEC)</description>
    <description languageCode="sv">Klass AIMDD för medicintekniska produkter (enligt EU-direktiv AIMDD 90/385/EEG)</description>
</code>
<code>
    <value>EU_CLASS_I</value>
    <name languageCode="sv">Klass I medicinteknisk produkt – Lågrisk</name>
    <name languageCode="en">Class I Medical Device - Low-risk</name>
    <description languageCode="en">Class EU_CLASS_I for Medical Devices (according to EU Directives MDD 93/42/EEC )</description>
    <description languageCode="sv">Klass EU_CLASS_I för medicintekniska produkter (enligt EU-direktiv MDD 93/42/EEG)</description>
</code>
<code>
    <value>EU_CLASS_IIA</value>
    <name languageCode="sv">Klass IIA medicinteknisk produkt – Låg-mellanrisk</name>
    <name languageCode="en">Class IIA Medical Device - Low-medium risk</name>
    <description languageCode="en">Class EU_CLASS_IIA for Medical Devices (according to EU Directives MDD 93/42/EEC )</description>
    <description languageCode="sv">Klass EU_CLASS_IIA för medicintekniska produkter (enligt EU-direktiv MDD 93/42/EEG)</description>
</code>
<code>
    <value>EU_CLASS_IIB</value>
    <name languageCode="sv">Klass IIB medicinteknisk produkt – Mellan-högrisk</name>
    <name languageCode="en">Class IIB Medical Device - Medium-high risk</name>
    <description languageCode="en">Class EU_CLASS_IIB for Medical Devices (according to EU Directives MDD 93/42/EEC )</description>
    <description languageCode="sv">Klass EU_CLASS_IIB för medicintekniska produkter (enligt EU-direktiv MDD 93/42/EEG)</description>
</code>
<code>
    <value>EU_CLASS_III</value>
    <name languageCode="sv">Klass III medicinteknisk produkt – Högrisk</name>
    <name languageCode="en">Class III Medical Device - High-risk</name>
    <description languageCode="en">Class EU_CLASS_III for Medical Devices (according to EU Directives MDD 93/42/EEC )</description>
    <description languageCode="sv">Klass EU_CLASS_III för medicintekniska produkter (enligt EU-direktiv MDD 93/42/EEG)</description>
</code>
<code>
    <value>IVDD_ANNEX_II_LIST_A</value>
    <name languageCode="sv">IVDD Bilaga II Lista A</name>
    <name languageCode="en">IVDD Annex II List A</name>
    <description languageCode="en">IVDD Annex II List A as specified in European In Vitro Diagnostic Devices Directive (IVDD 98/79/EC)</description>
    <description languageCode="sv">IVDD Bilaga II Lista A enligt europeiska direktivet om medicintekniska produkter för in vitro-diagnostik (IVDD 98/79/EG)</description>
</code>
<code>
    <value>IVDD_ANNEX_II_LIST_B</value>
    <name languageCode="sv">IVDD Bilaga II Lista B</name>
    <name languageCode="en">IVDD Annex II List B</name>
    <description languageCode="en">IVDD Annex II List B as specified in European In Vitro Diagnostic Devices Directive (IVDD 98/79/EC)</description>
    <description languageCode="sv">IVDD Bilaga II Lista B enligt europeiska direktivet om medicintekniska produkter för in vitro-diagnostik (IVDD 98/79/EG)</description>
</code>
<code>
    <value>IVDD_DEVICES_SELF_TESTING</value>
    <name languageCode="sv">IVDD-produkter för självtestning</name>
    <name languageCode="en">IVDD devices for self-testing</name>
    <description languageCode="en">Class EU_CLASS_SelfTest for In-Vitro Diagnostic Devices (according to EU Directive IVDD 98/79/EEC)</description>
    <description languageCode="sv">Klass EU_CLASS_SelfTest för in vitro-diagnostiska produkter (enligt EU-direktiv IVDD 98/79/EEG)</description>
</code>
<code>
    <value>IVDD_GENERAL</value>
    <name languageCode="sv">IVDD Allmänt</name>
    <name languageCode="en">IVDD General</name>
    <description languageCode="en">Class EU_CLASS_General for In-Vitro Diagnostic Devices (according to EU Directive IVDD 98/79/EEC)</description>
    <description languageCode="sv">Klass EU_CLASS_General för in vitro-diagnostiska produkter (enligt EU-direktiv IVDD 98/79/EEG)</description>
</code>
	</codeList>
