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STA® - Liquid Fib - India CDSCO Medical Device Registration

STA® - Liquid Fib is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/001107_c6cb6e9e534dc1f47fd76fb9bdd5ffb0_2cd982c10d527f7f2a035b40f584bbff. This device is marketed under the brand name STAGO. The license holder is Imperial Biotek, and it is classified as Device Class Class C. 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 C
STA® - Liquid Fib
UID: IMP/IVD/2020/001107_c6cb6e9e534dc1f47fd76fb9bdd5ffb0_2cd982c10d527f7f2a035b40f584bbff

Brand Name

STAGO

License Holder

Imperial Biotek

Device Class

Class C

Approving Authority

CDSCO

Product Information

Quantitative Determination of Fibrinogen

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