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                        <title>WI A00008:10:079866. ISO 18113-1:2022 - In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements</title>
                        <description>Projekts sasniedzis stadiju 60.60 datumā 06.10.2022. Atbildīgā komiteja: ISO/TC 212/WG 3. ICS: 11.100.10</description>
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                        <pubDate>Fri, 08 Nov 2019 13:42:05 +0200</pubDate>
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                        <title>WI A00008:10:079867. ISO 18113-2:2022 - In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use</title>
                        <description>Projekts sasniedzis stadiju 60.60 datumā 06.10.2022. Atbildīgā komiteja: ISO/TC 212/WG 3. ICS: 11.100.10</description>
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                        <pubDate>Fri, 08 Nov 2019 13:42:05 +0200</pubDate>
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                        <title>WI A00008:10:079868. ISO 18113-3:2022 - In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use</title>
                        <description>Projekts sasniedzis stadiju 60.60 datumā 06.10.2022. Atbildīgā komiteja: ISO/TC 212/WG 3. ICS: 11.100.10</description>
                        <link>https:/www.lvs.lv/projects/project/363409</link>
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                        <pubDate>Fri, 08 Nov 2019 13:42:04 +0200</pubDate>
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                        <title>WI A00008:10:079869. ISO 18113-4:2022 - In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing</title>
                        <description>Projekts sasniedzis stadiju 60.60 datumā 06.10.2022. Atbildīgā komiteja: ISO/TC 212/WG 3. ICS: 11.100.10</description>
                        <link>https:/www.lvs.lv/projects/project/363408</link>
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                        <pubDate>Fri, 08 Nov 2019 13:42:04 +0200</pubDate>
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                        <title>WI A00008:10:079870. ISO 18113-5:2022 - In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing</title>
                        <description>Projekts sasniedzis stadiju 60.60 datumā 06.10.2022. Atbildīgā komiteja: ISO/TC 212/WG 3. ICS: 11.100.10</description>
                        <link>https:/www.lvs.lv/projects/project/363407</link>
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                        <pubDate>Fri, 08 Nov 2019 13:41:59 +0200</pubDate>
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