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Progesterone CLIA - India CDSCO Medical Device Registration

Progesterone CLIA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000015_fdb8913b8c1e0a7f8e579278a9d1bc5d_2301f5cb6b1aa95e7c0231b84c79cf3c. The license holder is ASPEN LABORATORIES PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is North West Delhi 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
Progesterone CLIA
UID: MFG/IVD/2020/000015_fdb8913b8c1e0a7f8e579278a9d1bc5d_2301f5cb6b1aa95e7c0231b84c79cf3c

Device Class

Class B

Approving Authority

North West Delhi Division

Product Information

Chemiluminescent Immunoassay ##PLACEHOLDER_0## for the quantitative determination of progesterone ##PLACEHOLDER_0## in human serum

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