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RAPID PLASMA REAGIN TEST KIT - India CDSCO Medical Device Registration

RAPID PLASMA REAGIN TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000077_a3a8e5492a1b564fe6a5d0cc92b3c732_d96201ac76cfe915f19c47c1c93f70d0. This device is marketed under the brand name RECOMBIGEN. The license holder is RECOMBIGEN LABORATORIES PVT. LTD, 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.

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CDSCO Registered
Class Class B
RAPID PLASMA REAGIN TEST KIT
UID: MFG/MD/2019/000077_a3a8e5492a1b564fe6a5d0cc92b3c732_d96201ac76cfe915f19c47c1c93f70d0

Brand Name

RECOMBIGEN

Device Class

Class B

Approving Authority

North West Delhi Division

Product Information

The RPR Carbon Reagent is a stabilized suspension of cholesterol crystals coated by cardiolipin lecithin added to adjust the sensitivity and charcoal particles to improve the reading of the reaction. The reagents act as antigen against antibodies presents in persons suffering from syphilis. These antibodies are called โ€œ Reaginsโ€

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