COVID-19 IgG ELISA Kit - India CDSCO Medical Device Registration

COVID-19 IgG ELISA Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000034_73e57c613f0b49310bf5841d4adce929_9474f5a2288b58cd6c3d61dcc54b5f4b. This device is marketed under the brand name Aridia. The license holder is Athenese-Dx Private Limited, and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.

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CDSCO Registered

Class Class C

COVID-19 IgG ELISA Kit

UID: MFG/IVD/2020/000034_73e57c613f0b49310bf5841d4adce929_9474f5a2288b58cd6c3d61dcc54b5f4b

Brand Name

Aridia

License Holder

Athenese-Dx Private Limited

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

The TRUSTwell COVID-19 IgG ELISA Kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of COVID-19 IgG antibodies in human serum or plasma.

Class C

Brand: TRUSTline

Class D