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Covid19 IgG Antibody Elisa Test - India CDSCO Medical Device Registration

Covid19 IgG Antibody Elisa Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000026_e191725b72e54a7b91d7aa04a2e8a847_60e1c3789933bc9b52fccbc89c77506b. This device is marketed under the brand name Bhat Bio-Scan. The license holder is Bhat Bio-Tech India Private Limited, and it is classified as Device Class Class D. The approving authority is Sub Zonal Bangalore.

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 D
Covid19 IgG Antibody Elisa Test
UID: MFG/IVD/2022/000026_e191725b72e54a7b91d7aa04a2e8a847_60e1c3789933bc9b52fccbc89c77506b

Brand Name

Bhat Bio-Scan

Device Class

Class D

Approving Authority

Sub Zonal Bangalore

Product Information

Bhat Bio-Scan COVID-19 IgG Elisa test is an in-vitro enzyme immuno assay for the detection of IgG Antibodies to COVID-19 in Human Serum / Plasma.

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