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PHOSPHORUS liquirapid - India CDSCO Medical Device Registration

PHOSPHORUS liquirapid is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_cd89ee29650b871afb35fdaac9db255e_8bb7303a3b46f6ad685f7a18273708bd. 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
PHOSPHORUS liquirapid
UID: IMP/IVD/2019/000206_cd89ee29650b871afb35fdaac9db255e_8bb7303a3b46f6ad685f7a18273708bd

Device Class

Class B

Approving Authority

CDSCO

Product Information

PHOSPHORUS liquirapid is a Photometric UV Test for the Determination of Phosphorus and has been designed for the quantitative determination of inorganic phosphorus in human serum

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