Rubella Detection Kit - India CDSCO Medical Device Registration

Rubella Detection Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000021_9938bf62c8d06b2267bdaccfe99038d0_ec0e9a379c9cc185dd170fc980fd433f. This device is marketed under the brand name Multigene-Multiplex Single tube format. The license holder is Mylab Discovery S0lutions Pvt. Ltd, and it is classified as Device Class Class C. 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 C

Rubella Detection Kit

UID: MFG/IVD/2020/000021_9938bf62c8d06b2267bdaccfe99038d0_ec0e9a379c9cc185dd170fc980fd433f

Brand Name

Multigene-Multiplex Single tube format

License Holder

Mylab Discovery S0lutions Pvt. Ltd

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Rubella Detection kit is an in vitro nucleic acid amplification test for detection of Rubella RNA in various types of clinical samples of human origin. This diagnostic test kit utilizes the real time polymerase chain reaction (Multigene-Multiplex Single tube format) after nucleic acid extraction

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Brand: Multigene-Multiplex Single tube format

Mylab Discovery S0lutions Pvt. Ltd

Rubella Detection Kit - India CDSCO Medical Device Registration

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License Holder

Device Class

Approving Authority

Product Information

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