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DIAGNOSTICS TEST REAGENT/ KITS FOR TROPONIN I - India CDSCO Medical Device Registration

DIAGNOSTICS TEST REAGENT/ KITS FOR TROPONIN I is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000009_44dd7e01fb71097ef8eb9bba8234cc74_d68c306419d06df1ce2ee29bf7fcff9b. This device is marketed under the brand name Covid-19 RT PCR. The license holder is Vimek Bioconcept Pvt Ltd, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West Zone.

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CDSCO Registered
Class Class C
DIAGNOSTICS TEST REAGENT/ KITS FOR TROPONIN I
UID: MFG/IVD/2022/000009_44dd7e01fb71097ef8eb9bba8234cc74_d68c306419d06df1ce2ee29bf7fcff9b

Brand Name

Covid-19 RT PCR

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Rapid test for Troponin I - Device/Cassetteโ€ is an Lateral flow assay for the rapid and visual detection of Troponin I ( Covid-19 RT PCR) in human serum/plasma/ whole blood for the diagnosis of myocardial Infarction.

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