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Rapid Immunochromatography Lateral Flow Test for H.Pylori Ag in human serum/plasma/whole blood - India CDSCO Medical Device Registration

Rapid Immunochromatography Lateral Flow Test for H.Pylori Ag in human serum/plasma/whole blood is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000068_7a9ed10931cb9c1df9fc30f67a6b4a9a_a7db36fa8f56265ec6e4b7133b969292. This device is marketed under the brand name Cassette format. The license holder is Biogenix Inc. Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.

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CDSCO Registered
Class Class C
Rapid Immunochromatography Lateral Flow Test for H.Pylori Ag in human serum/plasma/whole blood
UID: MFG/IVD/2020/000068_7a9ed10931cb9c1df9fc30f67a6b4a9a_a7db36fa8f56265ec6e4b7133b969292

Brand Name

Cassette format

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

For detection of H.Pylori Antigen in human serum and plasma

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