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LDH TEST KIT - India CDSCO Medical Device Registration

LDH TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000065_edbe64914f3c6bd65c3cc6cfbd35bd7e_360e92e06561bd837a5261fac82db3f7. The license holder is PRECILAB REAGENTS AND CHEMICALS PVT.LTD., and it is classified as Device Class Class B. The approving authority is Kokan 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
LDH TEST KIT
UID: MFG/IVD/2023/000065_edbe64914f3c6bd65c3cc6cfbd35bd7e_360e92e06561bd837a5261fac82db3f7

Device Class

Class B

Approving Authority

Kokan Division

Product Information

FOR ESTIMATION OF LDH IN SERUM OR PLASMA

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