SSY Group Limited announced on 6 May 2026 that its Full-range C-reactive protein (hsCRP + conventional CRP) Test Kit and Serum Amyloid A / C-reactive protein (SAA/CRP) Test Kit have received medical device registration certificates from the Hebei Provincial Drug Administration of China.
The Full-range CRP Test Kit, based on fluorescent immunochromatography, enables in-vitro quantitative detection of C-reactive protein levels in whole blood, serum and plasma, supporting clinical diagnosis of non-specific inflammation and cardiovascular diseases.
The SAA/CRP Test Kit, also employing fluorescent immunochromatography, quantitatively measures serum amyloid A and C-reactive protein in human serum, plasma or whole blood, and is intended as an adjunct diagnostic tool for non-specific inflammation.
Management highlighted that successive approvals of multiple test kits have opened a new pathway for the Group’s medical device product line.
The announcement was released as a voluntary update to inform shareholders and potential investors of the latest product development progress.
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