Pure Global

Dengue NS1 Ag Microwell ELISA - India CDSCO Medical Device Registration

Dengue NS1 Ag Microwell ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000133_c5fde8eae75456befd41f4d689395684_567e0ead750befb4b87d760552d6bdfb. This device is marketed under the brand name BeneSphera. The license holder is M/s Avantor Performance Materials India Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.

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 C
Dengue NS1 Ag Microwell ELISA
UID: MFG/IVD/2023/000133_c5fde8eae75456befd41f4d689395684_567e0ead750befb4b87d760552d6bdfb

Brand Name

BeneSphera

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Enzyme linked immunosorbent Assay for the qualitative detection of surface antigen to Dengue virus (BeneSphera) in human serum and plasma

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing