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qSARS-CoV-2 IgG/IgM Rapid Test - India CDSCO Medical Device Registration

qSARS-CoV-2 IgG/IgM Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000304_042c7727aefb19ff73b26f73740faa14_f6ed894c3bcb8d87160ef8d745f94add. This device is marketed under the brand name Cellex. The license holder is Concept Healthcare, and it is classified as Device Class Class C. 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 C
qSARS-CoV-2 IgG/IgM Rapid Test
UID: IMP/IVD/2020/000304_042c7727aefb19ff73b26f73740faa14_f6ed894c3bcb8d87160ef8d745f94add

Brand Name

Cellex

License Holder

Concept Healthcare

Device Class

Class C

Approving Authority

CDSCO

Product Information

The qSARS-CoV-2 IgG/IgM Rapid Test is intended for rapid and qualitative detection of antibodies indicative of SARS-CoV-2 infection and used as an aid for diagnosis of SARS-CoV-2 infection.

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