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LDH Liquid Stable - India CDSCO Medical Device Registration

LDH Liquid Stable is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000023_e9e3d31c153f7e9000000c811cfd4254_54911cbf960d3cbe5638558ab4c21f9b. This device is marketed under the brand name AUTOPAK™. The license holder is Siemens Healthcare Private Limited, and it is classified as Device Class Class B. The approving authority is Gujarat.

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 Liquid Stable
UID: MFG/MD/2018/000023_e9e3d31c153f7e9000000c811cfd4254_54911cbf960d3cbe5638558ab4c21f9b

Brand Name

AUTOPAK™

Device Class

Class B

Approving Authority

Gujarat

Product Information

LDH Liquid Stable assay Kits is for in vitro diagnostics use in the quantitative determinations of Lactate dehydrogenase (AUTOPAK™) activity in Human serum and plasma sample

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