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CDSCO UID MFG/IVD/2022/000049_1eae2ccdc4b0a1107f727d89bd14a90b_a64e8fb5d4205787b15eecc5df4f4528

COVID 19 RT-qPCR

Promea Therapeutics Private Limited·Device Class Class C·India CDSCO·Brand: ProPCR
Registration details
UID
MFG/IVD/2022/000049_1eae2ccdc4b0a1107f727d89bd14a90b_a64e8fb5d4205787b15eecc5df4f4528
Device class
Class C
Brand name
ProPCR
License holder
Promea Therapeutics Private Limited
Approving authority
CDSCO, Zonal office, Hyderabad
Product information
It is used to detect target gene amplification through gene specific primers and probes by using Taq Man Chemistry Method
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About this record

COVID 19 RT-qPCR is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000049_1eae2ccdc4b0a1107f727d89bd14a90b_a64e8fb5d4205787b15eecc5df4f4528. This device is marketed under the brand name ProPCR. The license holder is Promea Therapeutics Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO, Zonal office, Hyderabad.

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