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Adenosine Deaminase - India CDSCO Medical Device Registration

Adenosine Deaminase is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000023_d592cbb9a4a50a63f4be584f5dabc9b7_988b85a0528d65ed435f382f61f1207b. 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
Adenosine Deaminase
UID: MFG/MD/2018/000023_d592cbb9a4a50a63f4be584f5dabc9b7_988b85a0528d65ed435f382f61f1207b

Brand Name

AUTOPAK™

Device Class

Class B

Approving Authority

Gujarat

Product Information

Adenosine Deaminase (AUTOPAK™) assay Kits is for in vitro diagnostics use in the quantitative determinations of Adenosine deaminase activity in serum, plasma, pleural fluid and cerebrospinal Fluid sample

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