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STANDARD M10 Sputum Pretreatment Kit - India CDSCO Medical Device Registration

STANDARD M10 Sputum Pretreatment Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000339_854ae5de633fefabb9838f8aaeea1efd_4757d6d5a2a3295d2c5cf83869945884. The license holder is SD Biosensor Healthcare 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
STANDARD M10 Sputum Pretreatment Kit
UID: IMP/IVD/2023/000339_854ae5de633fefabb9838f8aaeea1efd_4757d6d5a2a3295d2c5cf83869945884

Device Class

Class B

Approving Authority

CDSCO

Product Information

STANDARD M10 Sputum Pretreatment Kit is used to liquefy and pretreat the sputum specimen before processing for downstream nucleic acid extraction and molecular diagnostic testing

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