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17OH Progesterone ELISA - India CDSCO Medical Device Registration

17OH Progesterone ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000212_e8ea0697c6baedd867107c164a38167c_a06afee312070b7acc7b7049cc576aba. This device is marketed under the brand name DiaMetra. The license holder is Weldon Biotech India Pvt. Ltd, 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
17OH Progesterone ELISA
UID: IMP/IVD/2023/000212_e8ea0697c6baedd867107c164a38167c_a06afee312070b7acc7b7049cc576aba

Brand Name

DiaMetra

Device Class

Class B

Approving Authority

CDSCO

Product Information

17OH Progesterone ELISA is a manual in vitro diagnostic device intended for the quantitative determination of 17OH Progesterone in human serum or plasma

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