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Urine CrossLaps® EIA - India CDSCO Medical Device Registration

Urine CrossLaps® EIA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000273_278e8777aaf91e269d7fc0bf0eb0be73_d08de91200ad6ff2f88df2bed55e1be2. 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 CrossLaps® EIA
UID: IMP/IVD/2023/000273_278e8777aaf91e269d7fc0bf0eb0be73_d08de91200ad6ff2f88df2bed55e1be2

Brand Name

IDS

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Urine CrossLaps® (IDS)EIA is an enzyme immunosorbent assay for quantitative determination of degradation products of C-terminal telopeptides of Type-I collagen in human urine

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