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GLYCOHEMOGLOBIN TEST KIT - India CDSCO Medical Device Registration

GLYCOHEMOGLOBIN TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000023_f070ec9c78e90565b330026b74678eb0_b7442bdb6b0f7136550eb436cf5a7679. This device is marketed under the brand name A1Chek. The license holder is TULIP DIAGNOSTICS 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
GLYCOHEMOGLOBIN TEST KIT
UID: IMP/IVD/2023/000023_f070ec9c78e90565b330026b74678eb0_b7442bdb6b0f7136550eb436cf5a7679

Brand Name

A1Chek

Device Class

Class B

Approving Authority

CDSCO

Product Information

In-vitro diagnostic kits used in Glycohemoglobin test.

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