Serum CrossLaps® ELISA - India CDSCO Medical Device Registration
Serum CrossLaps® ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000273_804ab803d4a1d94ea35ccaa21cd6d9ab_37ef9b528eb2af93d960f8562313746a. 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.
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Brand Name
IDS
License Holder
Weldon Biotech India Pvt. LtdDevice Class
Approving Authority
CDSCO
Product Information
The Serum CrossLaps® (IDS) ELISA is an enzyme immunological test for the quantification of degradation products of C terminal telopeptides of Type I collagen in human serum and plasma. The Serum CrossLaps® (IDS) ELISA assay is intended for in vitro diagnostic use as an indication of human bone resorption
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