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UREA REAGENT(ERBA UREA KIT) - India CDSCO Medical Device Registration

UREA REAGENT(ERBA UREA KIT) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000042_e1b78675e601f6ef1d2935f2fa89d7bd_7e5c7564e8e783e59e18b5f0e9efb55f. This device is marketed under the brand name LIQUIXX -M- URIC ACID. The license holder is Transasia Bio-Medicals Limited, and it is classified as Device Class Class B. The approving authority is Solan(BBN).

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 REAGENT(ERBA UREA KIT)
UID: MFG/IVD/2022/000042_e1b78675e601f6ef1d2935f2fa89d7bd_7e5c7564e8e783e59e18b5f0e9efb55f

Brand Name

LIQUIXX -M- URIC ACID

Device Class

Class B

Approving Authority

Solan(BBN)

Product Information

BUN reagent, when used in conjunction with XL Multi Calibrator OR Urea standard, is intended for the quantitative determination of Urea Nitrogen concentration in human serum, plasma or urine

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