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Reagent Pack - India CDSCO Medical Device Registration

Reagent Pack is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000398_c10af154a4ece67606c2f3136fb42be0_0e81ef7fc8c852e20acf2a1909f93fea. This device is marketed under the brand name Reagent Pack. The license holder is Trivitron Healthcare Pvt. Ltd., 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
Reagent Pack
UID: IMP/IVD/2019/000398_c10af154a4ece67606c2f3136fb42be0_0e81ef7fc8c852e20acf2a1909f93fea

Brand Name

Reagent Pack

Device Class

Class B

Approving Authority

CDSCO

Product Information

Used for the quantitative determination of Sodium, Potassium, Chloride or Lithium in serum, plasma, urine, whole blood & CSF using the Biolyte analyzer. For in vitro diagnostic use only

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