WBC LYSE - India CDSCO Medical Device Registration

WBC LYSE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000419_89b71ada39e1430b35f3f975ee4ab51f_71917b54223f56d5ef5eec0cc23b49c3. This device is marketed under the brand name DILUENT/SHEATH. The license holder is Abbott Healthcare 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

WBC LYSE

UID: IMP/IVD/2019/000419_89b71ada39e1430b35f3f975ee4ab51f_71917b54223f56d5ef5eec0cc23b49c3

Brand Name

DILUENT/SHEATH

License Holder

Abbott Healthcare Pvt. Ltd.

Device Class

Class B

Approving Authority

CDSCO

Product Information

Act as the diluent for the WBC. Osmotically lyse the red cells. Act as a diluent for Reticulocytes

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WBC LYSE

Brand: WBC Reagent, PART B

Abbott Healthcare Pvt. Ltd.

WBC LYSE - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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