Enzyme-linked Immunosorbent Assay for Quantitative Determination of Procalcitonin in Human serum/plasma
- UID
- MFG/IVD/2019/000013_e22fedfc0973ec610521eb9fb77bacc6_d9d3a69a25ca4f5cf23aca4e9696ad04
- Device class
- Class B
- Brand name
- PCT
- Approving authority
- Goa
- Product information
- QUALISA PCT test is intended for the Enzyme linked Immunosorbent Assay (PCT) for Quantitative Determination of Procalcitonin (PCT) in Human Serum
Enzyme-linked Immunosorbent Assay for Quantitative Determination of Procalcitonin in Human serum/plasma is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000013_e22fedfc0973ec610521eb9fb77bacc6_d9d3a69a25ca4f5cf23aca4e9696ad04. This device is marketed under the brand name PCT. The license holder is QUALPRO DIAGNOSTICS A DIVISION OF TULIP DIAGNOSTICS PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is Goa.
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.