CDSCO UID IMP/IVD/2021/000312_f7cc31f648ef9d55ad26f5d4eae864bd_b8d205f26ad484b1d5ac5b25ec4dae90

5-Part-Diff Auto Hematology Analyzer()

Trivitron Healthcare Pvt. Ltd·Device Class Class A·India CDSCO·Brand: Cellenium 21 Hematology Analyzer
Registration details
UID
IMP/IVD/2021/000312_f7cc31f648ef9d55ad26f5d4eae864bd_b8d205f26ad484b1d5ac5b25ec4dae90
Device class
Class A
Brand name
Cellenium 21 Hematology Analyzer
Approving authority
CDSCO
Product information
5-Part-Diff Auto Hematology Analyzer is for blood cell count, WBC five-part differential and hemoglobin concentration measurement in clinical laboratory.
Similar products (1)
Other products with the same name or brand
Automated Hematology Analyzer
Brand: Cellenium 21 Hematology Analyzer
Trivitron Healthcare Pvt. Ltd
Class A
Other products from Trivitron Healthcare Pvt. Ltd
Products from the same license holder (10 products)
Neoscreen IRT EIA Kit
Brand: Immunoreactive Tripsinogen
Class C
Neoscreen hTSH EIA kit
Brand: Immunoreactive Tripsinogen
Class C
Syphilis Ab ELISA Kit
Brand: HBsAg ELISA Kit, Labsystems Diagnostics
Class D
HIV 1/2 RAPID TEST KIT
Brand: HBsAg ELISA Kit, Labsystems Diagnostics
Class D
D-dimer Test Reagent kit for Nanolab 200 Analyzer
Brand: Immunoreactive Tripsinogen
Class C
C-Reactive Protein Test Reagent kit
Brand: Immunoreactive Tripsinogen
Class C
COVID SCREEN PLUS ELISA kit
Brand: Immunoreactive Tripsinogen
Class C
COVID KAVACH Anti-SARS CoV-2 Human IgG ELISA kit
Brand: Immunoreactive Tripsinogen
Class C
COVIDSure Pro Multiplex RT PCR Kit
Brand: Immunoreactive Tripsinogen
Class C
HIV Ag-Ab ELISA Kit
Brand: HBsAg ELISA Kit, Labsystems Diagnostics
Class D
About this record

5-Part-Diff Auto Hematology Analyzer() is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000312_f7cc31f648ef9d55ad26f5d4eae864bd_b8d205f26ad484b1d5ac5b25ec4dae90. This device is marketed under the brand name Cellenium 21 Hematology Analyzer. The license holder is Trivitron Healthcare 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.