Description
Under current regulations, specimen collection cards, including neotal 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 93 specimen collection devices manufactured and printed by Whatman for neotal 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 93 collection devices converted, printed, or packaged by third party suppliers.
Specifications
| brand | Whatman |
|---|---|
| diameter-mm | 132.3 x 140 |
| manufacturer-part-number | WB100014 |
| part-number | WB100014 |
| quantity-per-pack | 100 |
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