BIOCARD Pro COVID-19 Rapid Antigen Test Kit - India CDSCO Medical Device Registration

BIOCARD Pro COVID-19 Rapid Antigen Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000053_68dd930046a5af903d0a3d8d3ab82ae6_0d22c2cf5669ec3c14088f2741db0fbf. This device is marketed under the brand name Immunoreactive Tripsinogen. The license holder is Trivitron Healthcare Pvt. Ltd, 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

BIOCARD Pro COVID-19 Rapid Antigen Test Kit

UID: MFG/IVD/2020/000053_68dd930046a5af903d0a3d8d3ab82ae6_0d22c2cf5669ec3c14088f2741db0fbf

Brand Name

Immunoreactive Tripsinogen

License Holder

Trivitron Healthcare Pvt. Ltd

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

BIOCARD Pro COVID-19 Rapid Antigen Test Kit is an in vitro diagnostic medical device based on Immuno-Chromatographic Assay (Immunoreactive Tripsinogen) for the qualitative detection of SARS-CoV-2 antigen in human nasopharyngeal specimens

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Neoscreen IRT EIA Kit

Brand: Immunoreactive Tripsinogen

Trivitron Healthcare Pvt. Ltd

BIOCARD Pro COVID-19 Rapid Antigen Test Kit - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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