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Creatinine FK - India CDSCO Medical Device Registration

Creatinine FK is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000131_ceaff15a753d3b72453fe5fd3bef7e19_76637f4a3e2d160e2a86af11e8b97f3e. This device is marketed under the brand name Rapid Widal. The license holder is BIOLAB DIAGNOSTICS (I) PVT. LTD., and it is classified as Device Class Class B. The approving authority is Kokan Division.

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
Creatinine FK
UID: MFG/IVD/2023/000131_ceaff15a753d3b72453fe5fd3bef7e19_76637f4a3e2d160e2a86af11e8b97f3e

Brand Name

Rapid Widal

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Creatinine (Rapid Widal) is used for the estimation of creatinine in serum/plasma

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