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Urine BETA CrossLaps ELISA - India CDSCO Medical Device Registration

Urine BETA CrossLaps ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000273_154201a505d915d8c41239e4a4ac5157_eee381478ded0292c4f05e7200c94edf. 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 BETA CrossLaps ELISA
UID: IMP/IVD/2023/000273_154201a505d915d8c41239e4a4ac5157_eee381478ded0292c4f05e7200c94edf

Brand Name

IDS

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Urine BETA CrossLaps® (IDS)ELISA is an enzyme immunological test for the quantification of degradation products of C-terminal telopeptides of Type-I collagen in human urine

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