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URIC ACID LIQUID - India CDSCO Medical Device Registration

URIC ACID LIQUID is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000502_ec919d9f62ec11dd126a6f9b4ae69fa4_aa417b202527f09d4d58f0a3a06a7147. This device is marketed under the brand name QCA. The license holder is ARK Diagnostic System 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
URIC ACID LIQUID
UID: IMP/IVD/2023/000502_ec919d9f62ec11dd126a6f9b4ae69fa4_aa417b202527f09d4d58f0a3a06a7147

Brand Name

QCA

Device Class

Class B

Approving Authority

CDSCO

Product Information

: For โ€œIn vitroโ€ determination of uric acid in serum, plasma or urine

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