CDSCO UID MFG/IVD/2023/000066_b62147570276c50f177941bd46d69642_c33a5f25acf6d806857d7826e1cf018f

Bilirubin Test Kit

Precilab Reagents And Chemicals Pvt Ltd·Device Class Class B·India CDSCO·Brand: Direct
Registration details
UID
MFG/IVD/2023/000066_b62147570276c50f177941bd46d69642_c33a5f25acf6d806857d7826e1cf018f
Device class
Class B
Brand name
Direct
Approving authority
Kokan Division
Product information
Photometric invitro estimation of Bilirubin in serum or plasma
Similar products (10)
Other products with the same name or brand
Bilirubin test kit
Brand: Direct
Precilab Reagents And Chemicals Pvt Ltd
Class B
Urea Test Kit
Brand: Direct
Precilab Reagents And Chemicals Pvt Ltd
Class B
LDL Cholesterol Test kit
Brand: Direct
Precilab Reagents And Chemicals Pvt Ltd
Class B
HDL Cholesterol Test Kit
Brand: Direct
Precilab Reagents And Chemicals Pvt Ltd
Class B
Bilirubin Test Kit
Brand: LordsMed Homocysteine Reagent
Lord's Mark Industries Pvt. Ltd.
Class B
Bilirubin Test Kit
Brand: Dir
Precilab Reagents And Chemicals Pvt. Ltd.
Class B
Bilirubin Test Kit
Brand: Dir
Precilab Reagents And Chemicals Pvt. Ltd.
Class B
Bilirubin Test Kit
Brand: Direct
Unicare Biomedical
Class B
Calcium Test Kit
Brand: Direct
Unicare Biomedical
Class B
HDL Cholesterol Test Kit
Brand: Direct
Unicare Biomedical
Class B
Other products from Precilab Reagents And Chemicals Pvt Ltd
Products from the same license holder (10 products)
Urea UV Test kit
Class B
Phosphorus Test Kit
Class B
Calcium Test Kit
Class B
Gamma GT Test kit
Class B
Bilirubin test kit
Brand: Direct
Class B
Triglycerides Test Kit
Class B
Glucose Test Kit
Class B
Potassium Test Kit
Class B
Diluent
Class B
Urea Test Kit
Brand: Direct
Class B
About this record

Bilirubin Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000066_b62147570276c50f177941bd46d69642_c33a5f25acf6d806857d7826e1cf018f. This device is marketed under the brand name Direct. The license holder is Precilab Reagents And Chemicals Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Kokan 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.