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Creatinine - India CDSCO Medical Device Registration

Creatinine is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000072_e33337def0a2ebfc1dfedc59a2970497_7b5f38510a06b0bc842196c84f5902b1. The license holder is Yucca Diagnostics, and it is classified as Device Class Class B. The approving authority is Pune 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
UID: MFG/IVD/2022/000072_e33337def0a2ebfc1dfedc59a2970497_7b5f38510a06b0bc842196c84f5902b1

License Holder

Yucca Diagnostics

Device Class

Class B

Approving Authority

Pune Division

Product Information

The Creatinine reagent kit is intended for the quantitative determination of Creatinine concentration in human serum or plasma using Modified Jaffeโ€™s Method. This kit is intended for professional in-vitro diagnostic use only

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