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UREA liquiUV - India CDSCO Medical Device Registration

UREA liquiUV is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_fadbb384ccbfcd124d4ea2ae3ee08492_c338f34d9f8a28da12064b7ebc000ee5. The license holder is Stedman Pharmaceuticals 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.

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CDSCO Registered
Class Class B
UREA liquiUV
UID: IMP/IVD/2019/000206_fadbb384ccbfcd124d4ea2ae3ee08492_c338f34d9f8a28da12064b7ebc000ee5

Device Class

Class B

Approving Authority

CDSCO

Product Information

UREA liquiUV reagent has been designed for the quantitative determination of urea in human serum, plasma, except ammonium heparinate plasma, or urine

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