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Urine CartiLaps® EIA - India CDSCO Medical Device Registration

Urine CartiLaps® EIA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000273_366625f485622f4170165065daf8b2bf_56c30ae84ed02f815c127ab1a4003a0c. This device is marketed under the brand name IDS. The license holder is Weldon Biotech India 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.

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CDSCO Registered
Class Class B
Urine CartiLaps® EIA
UID: IMP/IVD/2023/000273_366625f485622f4170165065daf8b2bf_56c30ae84ed02f815c127ab1a4003a0c

Brand Name

IDS

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Urine CartiLaps® (IDS) EIA is an enzyme immunological test for the quantification of degradation products of C-terminal telopeptides of Type II collagen in human urine

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