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ELISA Kit for detection of IgM antibodies to Rubella in Human serum/plasma - India CDSCO Medical Device Registration

ELISA Kit for detection of IgM antibodies to Rubella in Human serum/plasma is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000068_aa47733fcb8b6314730305d278282017_e81c27fbcd2816ad2f679d0575a6b14c. 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
ELISA Kit for detection of IgM antibodies to Rubella in Human serum/plasma
UID: MFG/IVD/2020/000068_aa47733fcb8b6314730305d278282017_e81c27fbcd2816ad2f679d0575a6b14c

Brand Name

Cassette format

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

A Rubella virus test reagent/kit is medical device intended for the detection of Rubella virus in serum/body fluids

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