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AR-9 Antigen Retrieval Solution - India CDSCO Medical Device Registration

AR-9 Antigen Retrieval Solution is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000059_6699a8a9f86f901bcfef59d477b66f7a_dccb9ac2b123bcfd0027bc89715f334d. This device is marketed under the brand name Typhoid IgG/IgM Rapid Test. The license holder is Dygnova Healthcare 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
AR-9 Antigen Retrieval Solution
UID: MFG/IVD/2023/000059_6699a8a9f86f901bcfef59d477b66f7a_dccb9ac2b123bcfd0027bc89715f334d

Brand Name

Typhoid IgG/IgM Rapid Test

Device Class

Class B

Approving Authority

Kokan Division

Product Information

AR-9 Solution is a commonly used Antigen Retrieval Solution intended for use in immunohistochemistry (Typhoid IgG/IgM Rapid Test) or Immunocytochemistry (Typhoid IgG/IgM Rapid Test) assays to improve the antigen retrieval of formalin-fixed, paraffin-embedded tissue sections

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