HEMOGLOBIN REAGENT KIT – MODIFIED ALKALINE HEMATIN METHOD - India CDSCO Medical Device Registration
HEMOGLOBIN REAGENT KIT – MODIFIED ALKALINE HEMATIN METHOD is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000072_f5d50a0023d85da27c18084c10c639cb_9cce21197d9602b51f7e7ca6a47c2338. This device is marketed under the brand name Ultichem. The license holder is Yucca Diagnostics, and it is classified as Device Class Class B. The approving authority is Pune Division.
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.
Brand Name
Ultichem
License Holder
Yucca DiagnosticsDevice Class
Approving Authority
Pune Division
Product Information
HEMOGLOBIN Kit is liquid stable reagent kit for the quantitative determination of HEMOGLOBIN in human Blood based on END POINT ALKLINE HEMATIN Method
SODIUM SINGLE REAGENT KIT - CHLOROPHOSPHANAZO METHOD
Brand: Ultichem
Yucca Diagnostics
CRP LATEX
Brand: Ultichem
Yucca Diagnostics
CRP REAGENT KIT
Brand: Ultichem
Yucca Diagnostics
BILIRUBIN REAGENT KIT - DMSO
Brand: Ultichem
Yucca Diagnostics
DILUENT REAGENT – FLOW CYTOMETRY METHOD
Brand: Ultichem
Yucca Diagnostics
GAMMA GT REAGENT KIT - IFCC KINETIC METHOD
Brand: Ultichem
Yucca Diagnostics
CREATININE SINGLE REAGENT KIT – JAFFE’S FIXED TIME KINETIC METHOD
Brand: Ultichem
Yucca Diagnostics
HbA1C REAGENT KIT – IMMUNO TURBIDIMETRIC METHOD
Brand: Ultichem
Yucca Diagnostics
BICARBONATE REAGENT KIT
Brand: Ultichem
Yucca Diagnostics
UREA REAGENT KIT – UREASE GLDH METHOD
Brand: Ultichem
Yucca Diagnostics

