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PHOSPHORUS liquirapid [HumaStar 300 SR, Humastar 600] - India CDSCO Medical Device Registration

PHOSPHORUS liquirapid [HumaStar 300 SR, Humastar 600] is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_ec0f16772e77bfdc215894a52e622cdf_45d0832c253e18c815376218dcf9b215. 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 [HumaStar 300 SR, Humastar 600]
UID: IMP/IVD/2019/000206_ec0f16772e77bfdc215894a52e622cdf_45d0832c253e18c815376218dcf9b215

Device Class

Class B

Approving Authority

CDSCO

Product Information

Photometric UV test for quantitative determination of inorganic phosphate in human serum on HumaStar 300 SR and HumaStar 600

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