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ALKALINE PHOSPHATASE - India CDSCO Medical Device Registration

ALKALINE PHOSPHATASE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000023_243ee4f97c61de420c745dbd949c6649_0da8ed58a531146b4ba6f6bf91a80c75. 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
ALKALINE PHOSPHATASE
UID: MFG/MD/2018/000023_243ee4f97c61de420c745dbd949c6649_0da8ed58a531146b4ba6f6bf91a80c75

Brand Name

AUTOPAK™

Device Class

Class B

Approving Authority

Gujarat

Product Information

For In vitro diagnostics use in quantitative determination of Alkaline Phosphatase in serum or plasma using clinical chemistry analyzer

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