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DS2 AUTOMATED ELISA SYSTEM - India CDSCO Medical Device Registration

DS2 AUTOMATED ELISA SYSTEM is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000410_b5f14c020714bce43c1e5c4e06ee0b10_040d63f68d1f01e3d1009be5614e2c7b. This device is marketed under the brand name DS2 AUTOMATED ELISA SYSTEM. The license holder is QIAGEN India Pvt. Ltd, and it is classified as Device Class Class A. 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 A
DS2 AUTOMATED ELISA SYSTEM
UID: IMP/IVD/2022/000410_b5f14c020714bce43c1e5c4e06ee0b10_040d63f68d1f01e3d1009be5614e2c7b

Brand Name

DS2 AUTOMATED ELISA SYSTEM

License Holder

QIAGEN India Pvt. Ltd

Device Class

Class A

Approving Authority

CDSCO

Product Information

DS2 is an analyzer with open functionality for processing chemical assays. It is the customerโ€™s sole responsibility to determine the DS2 systemโ€™s suitability for a particular Application, including any clinical application. DYNEX makes no representations, warranties or performance claims with respect to the performance of DS2 for any specific application, including clinical application or for the use of the DS2 system with any reagents, assays or other products. The customer is responsible for validating the system for its intended use.

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