Pure Global

CRP Turbi Latex - India CDSCO Medical Device Registration

CRP Turbi Latex is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000736_fa92ab6b02da4fbbfd73d447d5eb010a_d2de221d5c55a7f91346ffebbfdb04fd. This device is marketed under the brand name Spinreact. The license holder is ARK Diagnostic System Pvt.Ltd, and it is classified as Device Class Class C. 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 C
CRP Turbi Latex
UID: IMP/IVD/2020/000736_fa92ab6b02da4fbbfd73d447d5eb010a_d2de221d5c55a7f91346ffebbfdb04fd

Brand Name

Spinreact

Device Class

Class C

Approving Authority

CDSCO

Product Information

CRP-Turbilatex is a quantitative turbidimetric test for the measurement of Creactive protein (Spinreact) in human serum or plasma. Latex particles coated with specific anti- human CRP are agglutinated when mixed with samples containing CRP. The agglutination causes an absorbance change, dependent upon the CRP contents of the patient sample that can be quantified by comparison from a calibrator of known CRP concentration

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing