Erba Lisa® Syphilis - India CDSCO Medical Device Registration

Erba Lisa® Syphilis is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000014_4baa3e7bb1ef72a9850d7834399bacfc_acdd722f5a103543dddecd0c84aaf456. This device is marketed under the brand name ERBA LISA. The license holder is M/s.Transasia Bio-Medicals Ltd., and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.

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

Erba Lisa® Syphilis

UID: MFG/IVD/2020/000014_4baa3e7bb1ef72a9850d7834399bacfc_acdd722f5a103543dddecd0c84aaf456

Brand Name

ERBA LISA

License Holder

M/s.Transasia Bio-Medicals Ltd.

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Qualitative determination of total antibodies (ERBA LISA) to Treponema pallidum in human serum/plasma

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ERBA LISA HCV GEN4 Ag+Ab

Brand: ERBA LISA

M/s.Transasia Bio-Medicals Ltd.

Erba Lisa® Syphilis - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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ERBA LISA HCV GEN4 Ag+Ab

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ERBA LISA HIV GEN4 ver 2.0

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ERBA LISA HCV GEN3

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ERBA LISA HCV GEN3 VER 3.0

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ERBA LISA HIV GEN4 ver 2.0

Erba Lisa® SEN HBsAg

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ERBA LISA Dengue NS1 Ag

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