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IGE Test Kit - India CDSCO Medical Device Registration

IGE Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000127_6d6d73db16124017827a89fbb78e7f5b_1602c47749ab0b3b455aa57c4c8c5b5a. This device is marketed under the brand name POC T3. The license holder is Dygnova Healthcare Private Limited, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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 Test Kit
UID: MFG/IVD/2023/000127_6d6d73db16124017827a89fbb78e7f5b_1602c47749ab0b3b455aa57c4c8c5b5a

Brand Name

POC T3

Device Class

Class B

Approving Authority

Kokan Division

Product Information

IGE Test Kit (POC T3) for quantitative determination of IGE in Human Serum / Plasma / Whole blood,25-OH-VD Test Kit (POC T3)-25-OH-VD Test Kit (POC T3) for quantitative determination of 25-OH-VD in Human Serum / Plasma / Whole blood,mAlb Test Kit (POC T3)-mAlb Test Kit (POC T3) for quantitative determination of mAlb in Human Serum / Plasma / Whole blood

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