CDSCO UID IMP/IVD/2019/000040_babd24dbfaa5e717ac271ec19358a927_20d91046d0a2f0b79a8099dffaf87cf0

RF Latex

Beckman Coulter India Private Limited·Device Class Class B·India CDSCO·Brand: COULTER LH Series Pak Reagent Kit

Registration details

UID: IMP/IVD/2019/000040_babd24dbfaa5e717ac271ec19358a927_20d91046d0a2f0b79a8099dffaf87cf0
Device class: Class B
Brand name: COULTER LH Series Pak Reagent Kit
License holder: Beckman Coulter India Private Limited
Approving authority: CDSCO
Product information: Immuno-turbidimetric test for the quantitative determination of RF (COULTER LH Series Pak Reagent Kit) antibodies in human serum and plasma on Beckman Coulter AU analysers

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About this record

RF Latex is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000040_babd24dbfaa5e717ac271ec19358a927_20d91046d0a2f0b79a8099dffaf87cf0. This device is marketed under the brand name COULTER LH Series Pak Reagent Kit. The license holder is Beckman Coulter India Private Limited, and it is classified as Device Class Class B. The approving authority is CDSCO.

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