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LH ELISA - India CDSCO Medical Device Registration

LH ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2018/000005_729ac35b7eca0695e2a900676037dfbf_f70834872276a57f92d6dc0b89c6cfd2. This device is marketed under the brand name Pathozyme® Ultrasensitive TSH. The license holder is Omega DX (Asia) Private Limited, 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
LH ELISA
UID: IMP/IVD/2018/000005_729ac35b7eca0695e2a900676037dfbf_f70834872276a57f92d6dc0b89c6cfd2

Brand Name

Pathozyme® Ultrasensitive TSH

Device Class

Class B

Approving Authority

CDSCO

Product Information

Pathozyme® LH is an in-vitro diagnostic kit is used for the quantitative determination of Luteinizing Hormone (Pathozyme® Ultrasensitive TSH) in human serum

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