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AS DIRECT LATEX - India CDSCO Medical Device Registration

AS DIRECT LATEX is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000502_e349fbd7c06e488aa820bb26ceafcc97_98452b52446b3b4fb44d995ffac53434. This device is marketed under the brand name QCA. The license holder is ARK Diagnostic System Pvt.Ltd, and it is classified as Device Class Class B. The approving authority is CDSCO.

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
AS DIRECT LATEX
UID: IMP/IVD/2023/000502_e349fbd7c06e488aa820bb26ceafcc97_98452b52446b3b4fb44d995ffac53434

Brand Name

QCA

Device Class

Class B

Approving Authority

CDSCO

Product Information

For In vitro determination of anti-SLO antibodies in serum

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