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Fully Auto Glycated Hemoglobin Analyzer - India CDSCO Medical Device Registration

Fully Auto Glycated Hemoglobin Analyzer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000143_6e63825e386c68172262ad550dd3da76_1828da33e3c8f11ef274ec0262637f50. This device is marketed under the brand name B&E. The license holder is B & E Diagnostics India Private Limited, and it is classified as Device Class Class A. The approving authority is Gujarat.

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 A
Fully Auto Glycated Hemoglobin Analyzer
UID: MFG/IVD/2022/000143_6e63825e386c68172262ad550dd3da76_1828da33e3c8f11ef274ec0262637f50

Brand Name

B&E

Device Class

Class A

Approving Authority

Gujarat

Product Information

The HbA1c analyzer is used in combination with supporting reagents (B&E),using ion exchange high performance liquid chromatography (B&E) principle, for the quantitative detection of Hba1c in venous whole blood or peripheral blood samples in vitro

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