DIAGNOSTICS TEST REAGENT/ KITS FOR TROPONIN I
- UID
- MFG/IVD/2022/000009_44dd7e01fb71097ef8eb9bba8234cc74_d68c306419d06df1ce2ee29bf7fcff9b
- Device class
- Class C
- Brand name
- Covid-19 RT PCR
- License holder
- Vimek Bioconcept Pvt Ltd
- Approving authority
- Central Drug Standards Control Organization, West Zone
- Product information
- Rapid test for Troponin I - Device/Cassette” 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.
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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