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IgE rapid test - India CDSCO Medical Device Registration

IgE rapid test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000032_791b7714d68b059f87ae177af0268663_c1d4f011b9c91fc3e04758bb8f265d2b. This device is marketed under the brand name Paediatric version. The license holder is VORTEX MEDSOLUTIONS 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
IgE rapid test
UID: IMP/IVD/2020/000032_791b7714d68b059f87ae177af0268663_c1d4f011b9c91fc3e04758bb8f265d2b

Brand Name

Paediatric version

Device Class

Class B

Approving Authority

CDSCO

Product Information

IgE-CHECK-1 is a rapid qualitative test kit for the detection of IgE in whole blood, plasma or serum. The kit is intended for in vitro diagnostic use by health professionals.

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