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IGF-I (Maglumi IGF-I ) - India CDSCO Medical Device Registration

IGF-I (Maglumi IGF-I ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000036_c6ed51f7ba75069ec723e153dd6f6a6e_7fc99656d9fcdb6fed24dd0d8c3fba51. This device is marketed under the brand name MAGLUMI® Tip. The license holder is SNIBE DIAGNOSTIC (India) Private Limited., and it is classified as Device Class Class B. 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 B
IGF-I (Maglumi IGF-I )
UID: IMP/IVD/2023/000036_c6ed51f7ba75069ec723e153dd6f6a6e_7fc99656d9fcdb6fed24dd0d8c3fba51

Brand Name

MAGLUMI® Tip

Device Class

Class B

Approving Authority

CDSCO

Product Information

The kit is an in vitro chemiluminescence immunoassay for the quantitative determination of Insulin-like-growth factor 1 (MAGLUMI® Tip) in human serum and plasma

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