CDSCO UID IMP/IVD/2023/000392_7cdc37fc4feb65a300ee89f9a488a8ba_0716029117d9e860246b2b880f6c4754
NAISSA IGE
M/s Vishat Diagnostic Pvt Ltd.·Device Class Class B·India CDSCO
Registration details
- UID
- IMP/IVD/2023/000392_7cdc37fc4feb65a300ee89f9a488a8ba_0716029117d9e860246b2b880f6c4754
- Device class
- Class B
- License holder
- M/s Vishat Diagnostic Pvt Ltd.
- Approving authority
- CDSCO
- Product information
- "The test’s intended use is for quantitative determination of immunoglobulin E ##PLACEHOLDER_0## concentration in the human serum"
Other products from M/s Vishat Diagnostic Pvt Ltd.
Products from the same license holder (10 products)
Anti-dsDNA IgG
Class B
DHEA
Brand: E1
Class B
AMH
Class B
Anti-SS-B
Class B
Ferritin
Class B
NAISSA System liquid
Class B
NAISSA RSV IgM
Class B
Anti-SS-A
Class B
CCP IgG
Class B
PTH
Class B
About this record
NAISSA IGE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000392_7cdc37fc4feb65a300ee89f9a488a8ba_0716029117d9e860246b2b880f6c4754. The license holder is M/s Vishat Diagnostic Pvt 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.