Pure Global

CombiScreen® Dip Check - India CDSCO Medical Device Registration

CombiScreen® Dip Check is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000376_46724daf03184eb0c7df74ad8327d225_46c85003ac7ce21c4682e0968dc8295c. This device is marketed under the brand name CombiScreen®. The license holder is DiaSys Diagnostic India Private Limited, 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
CombiScreen® Dip Check
UID: IMP/IVD/2021/000376_46724daf03184eb0c7df74ad8327d225_46c85003ac7ce21c4682e0968dc8295c

Brand Name

CombiScreen®

Device Class

Class B

Approving Authority

CDSCO

Product Information

FOR IN VITRO DIAGNOSTIC USE CombiScreen® DIP Check is intended for use as an assayed quality control material for various urinalysis reagent strips and qualitative hCG methods. The list of various urinalysis reagent strips or analytes are : albumin, creatinine, ascorbic acid, bilirubin, blood, glucose, ketones, leucocytes, nitrite, pH-value, protein, specific gravity and urobilinogen in human urine

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing