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FOB Rapid Test Kit - India CDSCO Medical Device Registration

FOB Rapid Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000008_d05e810fd9ab004fdfce9f113f98d927_77acecbe8eb137721f98d1d0b6b43c95. This device is marketed under the brand name ARSENAZO METHOD. The license holder is BIOLINE DIAGNOSTICS LLP, and it is classified as Device Class Class B. The approving authority is North West Delhi Division.

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
FOB Rapid Test Kit
UID: MFG/IVD/2019/000008_d05e810fd9ab004fdfce9f113f98d927_77acecbe8eb137721f98d1d0b6b43c95

Brand Name

ARSENAZO METHOD

Device Class

Class B

Approving Authority

North West Delhi Division

Product Information

The FOB Rapid Test (ARSENAZO METHOD) is a rapid chromatographic immunoassay for the qualitative detection of human occult blood in feces

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