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HCG+Beta Fast Test Kit - India CDSCO Medical Device Registration

HCG+Beta Fast Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/001031_b1ba272c6de04f2a11be36151cd655a8_ca84ca889981576781c19fa508fe93c1. This device is marketed under the brand name Getein. The license holder is M/s. Peerless Biotech 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
HCG+Beta Fast Test Kit
UID: IMP/IVD/2020/001031_b1ba272c6de04f2a11be36151cd655a8_ca84ca889981576781c19fa508fe93c1

Brand Name

Getein

Device Class

Class B

Approving Authority

CDSCO

Product Information

HCG+Beta fast test kit (Getein) is intended for in vitro quantitative determination of human chorionic gonadotropin (Getein) in serum and plasma. This test is used as aid in pregnancy test

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