Testosterone Rapid Quantitative Test - India CDSCO Medical Device Registration
Testosterone Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000164_49e4d088ce9b113773c25dad781f26f6_8274402eb5401172f4d9fa4634c67e50. This device is marketed under the brand name E2. The license holder is M/s Avantor Performance Materials India Ltd, and it is classified as Device Class Class B. 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.
Brand Name
E2
License Holder
M/s Avantor Performance Materials India LtdDevice Class
Approving Authority
CDSCO
Product Information
Testosterone Rapid Quantitative Test is a fluorescence immunoassay used along with FinecareTM FIA Meters (E2) for quantitative measurement of Testosterone in human whole blood, serum or plasma. The test is to be used as an aid in the diagnosis of diseases related to abnormal testosterone levels.
Estradiol Rapid Quantitative Test
Brand: E2
Prolactin Rapid Quantitative Test
Brand: E2
AMH Rapid Quantitative Test
Brand: E2
SARS-CoV-2 RT-PCR Kit 1.0
Brand: RealStar®
FSH Test System
Brand: ELISA Kit
Free T4 Test System
Brand: ELISA Kit
Total T4 Test System
Brand: ELISA Kit
TSH Test System
Brand: ELISA Kit
LH Test System
Brand: ELISA Kit
PRL Test System
Brand: ELISA Kit