Regulation disclaimer – CE mark

Under current regulations, specimen collection cards, including neonatal screening cards, which are to be used for human diagnostic tests, are classified as "other" IVD devices under the European IVD Directive and require the CE mark if sold within the European Union. All 903 specimen collection devices manufactured and printed by Whatman for neonatal testing in the EU undergo post-printing quality control and carry the CE mark. Whatman will assume no responsibility for the quality or performance of 903 collection devices converted, printed, or packaged by third party suppliers.