HTLV I&II Ab Version ULTRA - India CDSCO Medical Device Registration

HTLV I&II Ab Version ULTRA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000842_71a45475d146292f5efbebfadefa7004_3b827bb0987345176b9b0d768c5aaf36. This device is marketed under the brand name HDV IgM. The license holder is Weldon Biotech India Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered

Class Class B

HTLV I&II Ab Version ULTRA

UID: IMP/IVD/2020/000842_71a45475d146292f5efbebfadefa7004_3b827bb0987345176b9b0d768c5aaf36

Brand Name

HDV IgM

License Holder

Weldon Biotech India Pvt. Ltd

Device Class

Class B

Approving Authority

CDSCO

Product Information

Enzyme Immunoassay for the qualitative determination of antibodies to Human T-Cell Lymphotropic Virus type I&II in serum and plasma

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HAV Ab

Brand: HDV IgM

Weldon Biotech India Pvt. Ltd

HTLV I&II Ab Version ULTRA - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

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