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Anti Human Globulin - India CDSCO Medical Device Registration

Anti Human Globulin is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000021_d9233f8171467de0a7a8c5a18fc195b8_7106cec4447d62ff908161454f43a57d. This device is marketed under the brand name RPR. The license holder is TULIP DIAGNOSTICS PRIVATE LIMITED, and it is classified as Device Class Class D. The approving authority is Sub Zonal Goa.

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 D
Anti Human Globulin
UID: MFG/IVD/2021/000021_d9233f8171467de0a7a8c5a18fc195b8_7106cec4447d62ff908161454f43a57d

Brand Name

RPR

Device Class

Class D

Approving Authority

Sub Zonal Goa

Product Information

Eryclone AHG, is used for compatibility testing, antibody detection, antibody identification, umbilical cord red blood testing and u detection of D variants of human red blood cell antigen D (RPR)

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