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Sensititre ARIS HiQ System - India CDSCO Medical Device Registration

Sensititre ARIS HiQ System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000053_3d56c8e939d67aee0006f329c0dd4b68_dbddd1736a470773aff348736b64f914. This device is marketed under the brand name Sensititre . The license holder is Thermo Fisher Scientific India Pvt. Ltd., and it is classified as Device Class Class A. The approving authority is CDSCO.

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CDSCO Registered
Class Class A
Sensititre ARIS HiQ System
UID: IMP/IVD/2023/000053_3d56c8e939d67aee0006f329c0dd4b68_dbddd1736a470773aff348736b64f914

Brand Name

Sensititre

Device Class

Class A

Approving Authority

CDSCO

Product Information

The ARIS HiQโ„ข system, the SWINโ„ข system, and these instructions for use are for the sole use of trained laboratory personnel for clinical, veterinary, industrial, and research use applications. Where used in a clinical setting, the intended use is The ARIS HiQโ„ข system is part of the Sensititreโ„ข system and is an automated read and incubation instrument for overnight (Sensititre ) in -vitro antimicrobial susceptibility testing of microorganism pathogens

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