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A Real Time PCR Test Kit for detection of Human Papillomaviruses (AMPLICHAIN HPV ) - India CDSCO Medical Device Registration

A Real Time PCR Test Kit for detection of Human Papillomaviruses (AMPLICHAIN HPV ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000134_305a21a5309e41cfcb2fce013b1f00c9_21be4fc09d50f2bfaab3816d38b5da86. This device is marketed under the brand name AMPLICHAIN Dengue/Chik V. The license holder is TULIP DIAGNOSTICS PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is Sub Zonal Goa.

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CDSCO Registered
Class Class C
A Real Time PCR Test Kit for detection of Human Papillomaviruses (AMPLICHAIN HPV )
UID: MFG/IVD/2022/000134_305a21a5309e41cfcb2fce013b1f00c9_21be4fc09d50f2bfaab3816d38b5da86

Brand Name

AMPLICHAIN Dengue/Chik V

Device Class

Class C

Approving Authority

Sub Zonal Goa

Product Information

Amplichain HPV (AMPLICHAIN Dengue/Chik V) is a real time PCR in-vitro diagnostic test kit intended for the qualitative detection of HPV (AMPLICHAIN Dengue/Chik V) virus from the clinical samples like blood/plasma in humans collected from individuals suspected of HPV (AMPLICHAIN Dengue/Chik V) infection by their healthcare provider

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