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SD BIOLINE Chikungunya IgM - India CDSCO Medical Device Registration

SD BIOLINE Chikungunya IgM is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000156_f0381fb3b4cdefcb0ae25c9d1555ecc3_26fb2e3fde50d8af9a141c65e1fe0f1a. This device is marketed under the brand name SD BIOLINE Dengue IgG/IgM WB. The license holder is Abbott Diagnostics Medical Private Limited, 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
SD BIOLINE Chikungunya IgM
UID: IMP/MD/2018/000156_f0381fb3b4cdefcb0ae25c9d1555ecc3_26fb2e3fde50d8af9a141c65e1fe0f1a

Brand Name

SD BIOLINE Dengue IgG/IgM WB

Device Class

Class B

Approving Authority

CDSCO

Product Information

SD BIOLINE Chikungunya IgM test is solid phase immunochromatographic assay for rapid, qualitative detection of IgM antibodies to Chikungunya in human serum, plasma or whole blood

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