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Devyser’s diagnostic kits are CE-IVD marked and used globally in over forty-five countries. The company has achieved IVDR Class D approval for its non-invasive fetal RHD product. It continues to expand regulatory approvals internationally—including China Class III approval—and seeks FDA clearance for its NGS kidney transplant monitoring test. Its products are widely adopted by clinical laboratories due to their speed, accuracy, ease of use, and ability to streamline complex genetic workflows.
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