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QUALICHECK PATH (QUALICHECK PATH ) - India CDSCO Medical Device Registration

QUALICHECK PATH (QUALICHECK PATH ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000005_f69793a48a3d57f10db3f992eeae68d1_4dc05fb204e2a19710cc9068977e497a. This device is marketed under the brand name Lp-PLA2 Reagent. The license holder is M/s. Agappe Diagnostics Ltd., and it is classified as Device Class Class B. The approving authority is Kerala.

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
QUALICHECK PATH (QUALICHECK PATH )
UID: MFG/IVD/2020/000005_f69793a48a3d57f10db3f992eeae68d1_4dc05fb204e2a19710cc9068977e497a

Brand Name

Lp-PLA2 Reagent

Device Class

Class B

Approving Authority

Kerala

Product Information

Qualicheck Path is an assayed human serum used for quality control checking of clinical chemistry assays suitable for manual procedure and automated analyzers

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