CDSCO UID IMP/IVD/2019/000398_c10af154a4ece67606c2f3136fb42be0_0e81ef7fc8c852e20acf2a1909f93fea

Reagent Pack

Trivitron Healthcare Pvt. Ltd.·Device Class Class B·India CDSCO·Brand: Reagent Pack

Registration details

UID: IMP/IVD/2019/000398_c10af154a4ece67606c2f3136fb42be0_0e81ef7fc8c852e20acf2a1909f93fea
Device class: Class B
Brand name: Reagent Pack
License holder: Trivitron Healthcare Pvt. Ltd.
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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About this record

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.

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