CDSCO UID IMP/IVD/2019/000206_e5005ac66d6076461ddcdbdfc46fd1e4_66ec4cc4109f7837ea76d1e95544debf

URIC ACID liquicolor plus

Stedman Pharmaceuticals Pvt. Ltd.·Device Class Class B·India CDSCO
Registration details
UID
IMP/IVD/2019/000206_e5005ac66d6076461ddcdbdfc46fd1e4_66ec4cc4109f7837ea76d1e95544debf
Device class
Class B
Approving authority
CDSCO
Product information
The Uric Acid liquicolor plus is a PAP-Method Enzymatic Colorimetric Test ##PLACEHOLDER_0## and has been designed for the quantitative determination of uric acid in human serum and plasma
Other products from Stedman Pharmaceuticals Pvt. Ltd.
Products from the same license holder (10 products)
UREA liquiUV
Class B
TRANSFERRIN HumaStar 600
Class B
PHOSPHORUS liquirapid [HumaStar 300 SR, Humastar 600]
Class B
LDL CHOLESTEROL liquicolor HumaStar 600
Class B
HbA1c liquidirect HumaStar 600
Class B
SODIUM liquicolor [HumaStar 300SR, HumaStar 600]
Class B
HC5D DIFF LYSE
Class B
MAGNESIUM liquicolor
Class B
HDL CHOLESTEROL liquicolor [HumaStar 300SR, HumaStar 600]
Class B
UREA liquiUV HumaStar 600
Class B
About this record

URIC ACID liquicolor plus is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_e5005ac66d6076461ddcdbdfc46fd1e4_66ec4cc4109f7837ea76d1e95544debf. The license holder is Stedman Pharmaceuticals Pvt. Ltd., and it is classified as Device Class Class B. 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.