PCT
- UID
- IMP/IVD/2019/000039_c1b9a5bfdcf1b4b586c4953afeff622b_f4ff6ff6ae6dec638848cd09d90b6133
- Device class
- Class C
- Brand name
- PCT Rapid Quantitative Test
- License holder
- M/s Avantor Performance Materials India Ltd
- Approving authority
- CDSCO
- Product information
- Quantitative determination of PCT in human whole blood, serum or plasma. This test is used as an aid to diagnosis severe, bacterial infection and sepsis. ,cTnI-NT proBNP(PCT Rapid Quantitative Test)-quantitative determination of cTn I and NT-proBNP in human whole blood, serum or plasma. This test is used as an aid to assist in the diagnosis of myocardial infarction and suspected congestive heart failure
PCT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000039_c1b9a5bfdcf1b4b586c4953afeff622b_f4ff6ff6ae6dec638848cd09d90b6133. This device is marketed under the brand name PCT Rapid Quantitative Test. The license holder is M/s Avantor Performance Materials India Ltd, and it is classified as Device Class Class C. The approving authority is CDSCO.
This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.