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Urine Diluent - India CDSCO Medical Device Registration

Urine Diluent is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000029_3b3ad410ccaaca52359218f083cdef57_5912da104fd0f156eb4993493d67ff2d. This device is marketed under the brand name SEROQUANT FERRITIN LEVEL I . The license holder is CORAL CLINICAL SYSTEMS A DIVISION OF TULIP DIAGNOSTICS PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is Goa.

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
Urine Diluent
UID: MFG/IVD/2022/000029_3b3ad410ccaaca52359218f083cdef57_5912da104fd0f156eb4993493d67ff2d

Brand Name

SEROQUANT FERRITIN LEVEL I

Device Class

Class B

Approving Authority

Goa

Product Information

For quantitative determination of Sodium, Chloride, and Potassium in Human urine sample on Electrolyte analyzer

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