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B (ERYCLONE ANTI - India CDSCO Medical Device Registration

B (ERYCLONE ANTI is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000021_f4027a38e5dbba4cf743d63bc5d93732_7fc56270e7a70fa81a5935b72eacbe29. 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
B (ERYCLONE ANTI
UID: MFG/IVD/2021/000021_f4027a38e5dbba4cf743d63bc5d93732_7fc56270e7a70fa81a5935b72eacbe29

Brand Name

RPR

Device Class

Class D

Approving Authority

Sub Zonal Goa

Product Information

A

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