Toxoplasma gondii test reagent/kit - India CDSCO Medical Device Registration

Toxoplasma gondii test reagent/kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000088_4fb5f383197f66526b937baa7bb83b71_f7769bd71f5cda87bd833aa78dbec40a. This device is marketed under the brand name ANGCARD. The license holder is Angstrom Biotech 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

Toxoplasma gondii test reagent/kit

UID: MFG/MD/2020/000088_4fb5f383197f66526b937baa7bb83b71_f7769bd71f5cda87bd833aa78dbec40a

Brand Name

ANGCARD

License Holder

Angstrom Biotech Pvt. Ltd.

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

To the detection of Toxoplasma Gondii in serum/body fluids

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Brand: HIV ½ card

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Brand: ANGCARD

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Brand: ANGCARD

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Brand: ANGCARD

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Brand: ANGCARD

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Brand: ANGCARD

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Brand: HIV ½ card

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Brand: HIV ½ card