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Anti Human C3d - India CDSCO Medical Device Registration

Anti Human C3d is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000021_c0e6009d62955e225fd461014c41de07_620181ed4773de5de2169f4e1423b349. This device is marketed under the brand name Monospecific Coombs Serum. The license holder is TULIP DIAGNOSTICS PRIVATE LIMITED, and it is classified as Device Class Class C. 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 C
Anti Human C3d
UID: MFG/IVD/2021/000021_c0e6009d62955e225fd461014c41de07_620181ed4773de5de2169f4e1423b349

Brand Name

Monospecific Coombs Serum

Device Class

Class C

Approving Authority

Sub Zonal Goa

Product Information

Eryclone Anti Human-C3d Monospecific Coombs reagent is a ready to use reagent containing antibodies reactive with human complement component C3d

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