Pure Global

Dengue IgG/IgM ELISA Kit - India CDSCO Medical Device Registration

Dengue IgG/IgM ELISA Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000015_f51455874628b77b68eab56a3425224c_161a29f4f2af7f0cf356afdeb10dc4df. The license holder is ASPEN LABORATORIES PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is North West Delhi Division.

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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Dengue IgG/IgM ELISA Kit
UID: MFG/IVD/2020/000015_f51455874628b77b68eab56a3425224c_161a29f4f2af7f0cf356afdeb10dc4df

Device Class

Class B

Approving Authority

North West Delhi Division

Product Information

Test kit for detection of Dengue IgG/IgM Antibodies

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name or brand