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Alpha CrossLaps® EIA - India CDSCO Medical Device Registration

Alpha CrossLaps® EIA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000273_2af2cc1ad4ebfd2a5c9ff0121fbc48a6_62a217e7995d0b062d656c24cabd2b98. 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
Alpha CrossLaps® EIA
UID: IMP/IVD/2023/000273_2af2cc1ad4ebfd2a5c9ff0121fbc48a6_62a217e7995d0b062d656c24cabd2b98

Brand Name

IDS

Device Class

Class B

Approving Authority

CDSCO

Product Information

The ALPHA CrossLaps® (IDS) EIA is an enzyme-linked immunosorbent assay for the quantification of nonisomerized fragments of C-terminal telopeptides of Type-I collagen (IDS) in human urine

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