Pure Global

Sensititre Nephelometer - India CDSCO Medical Device Registration

Sensititre Nephelometer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000053_40aa55a41b215077c0b2aad9d704e437_23f80b494f3ebee4c8ccb5b8ad9fb1bd. 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.

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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class A
Sensititre Nephelometer
UID: IMP/IVD/2023/000053_40aa55a41b215077c0b2aad9d704e437_23f80b494f3ebee4c8ccb5b8ad9fb1bd

Brand Name

Sensititre

Device Class

Class A

Approving Authority

CDSCO

Product Information

Thermo Scientificโ„ข Sensititreโ„ข Nephelometer is used for standardizing the inoculum density of a bacterial suspension. Light from an ultra-bright light emitting diode (Sensititre ) is scattered by bacteria in suspension and detected by a photodiode. The quantity of scattered light is compared with a reference value obtained by calibrating Nephelometer with a 0.5 McFarland turbidity standard

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing