Verify both targets on one product
A combined-panel product should be evaluated on its own stored analyte list. Do not assume that a cup includes EtG or fentanyl just because another cup from its series does, because its panel count is similar, or because a SKU contains an abbreviation.
The current catalog has specific records whose analyte lists include both EtG and fentanyl. Review each product’s specifications and package documentation to verify the version and requirements relevant to your organization.
Compare configuration details
Cup records can vary in panel count, additional checks, cutoff text, and other stored specifications. Compare those fields directly and retain the original wording. If the cutoff field and analyte list do not agree, ask for written clarification rather than treating a text token as confirmed coverage.
Product pages are aids for selection, not medical guidance. The actual test procedure and its limitations come from the documentation shipped with that specific product.
Make the purchasing decision traceable
Document the exact SKU, data source, requested targets, and any supplier clarification. Confirm current availability and pricing with the quote or ordering channel; this article does not promise inventory, turnaround, or a discounted price.
Program staff should determine how a presumptive screen fits their applicable procedures and which professional review may be needed.
