HP Ag - India CDSCO Medical Device Registration

HP Ag is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000842_ccfc0a88afece6043a494ae3012d828f_79972ebd4d28876d79e04cdba4aac443. This device is marketed under the brand name HDV IgM. The license holder is Weldon Biotech India 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.

Free Database

CDSCO Registered

Class Class B

HP Ag

UID: IMP/IVD/2020/000842_ccfc0a88afece6043a494ae3012d828f_79972ebd4d28876d79e04cdba4aac443

Brand Name

HDV IgM

License Holder

Weldon Biotech India Pvt. Ltd

Device Class

Class B

Approving Authority

CDSCO

Product Information

This device HP Ag is a quantitative/qualitative test to determination of Helicobacter pylori in human stool. The HPAG.CE test is intended exclusively for in vitro diagnostic use

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

HAV Ab

Brand: HDV IgM

Weldon Biotech India Pvt. Ltd

HP Ag - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

HAV Ab

HEV IgG

HP IgG

HDV IgM

HP IgM

T.Cruzi Ab

HTLV I&II Ab Version ULTRA

HP IgA

HAV IgM

CHIKV IgM

General Chemistry 9 Test Panel

Myocardial Enzyme Panel Test

Electrolyte 7 Test Panel

Liver Function Panel Test

Emergency Room 13 Test Panel

General Chemitry 13 Test Panel

Glucose and Lipid Panel Test

Renal Function Panel Test

Ostase® BAP EIA

BoneTRAP® ELISA