Pure Global

PRL Assay (PRL Assay ) - India CDSCO Medical Device Registration

PRL Assay (PRL Assay ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000207_f2b2dd19aef127b6db8e574f8ca7e124_5f38777136501ce327b0edfe038ff318. This device is marketed under the brand name CLIA. The license holder is Rapid House, 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
Powered by Pure Global AI
CDSCO Registered
Class Class B
PRL Assay (PRL Assay )
UID: IMP/IVD/2023/000207_f2b2dd19aef127b6db8e574f8ca7e124_5f38777136501ce327b0edfe038ff318

Brand Name

CLIA

License Holder

Rapid House

Device Class

Class B

Approving Authority

CDSCO

Product Information

PRL Assay (CLIA) is for the in vitro quantitative determination of prolactin in human serum and plasma

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing