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Anti-D IgM - India CDSCO Medical Device Registration

Anti-D IgM is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000021_d44f7de96bcd35bcf0adc2608c994255_38add330a60a4c597dce03e40c88213f. 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-D IgM
UID: MFG/IVD/2021/000021_d44f7de96bcd35bcf0adc2608c994255_38add330a60a4c597dce03e40c88213f

Brand Name

RPR

Device Class

Class D

Approving Authority

Sub Zonal Goa

Product Information

Eryclone Anti D (RPR) consists of blood grouping reagent for slide and modified tube tests. The reagent is murine monoclonal IgM for Rho (RPR) typing

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