VIASURE SARS-CoV-2 Real Time PCR Detection Kit - Indonesia BPOM Medical Device Registration
VIASURE SARS-CoV-2 Real Time PCR Detection Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303022701. The device is manufactured by CERTEST BIOTEC S.L. from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is STANDARD BIOSENSOR INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CERTEST BIOTEC S.L.Country of Origin
Spain
Authorized Representative
STANDARD BIOSENSOR INDONESIAAR Address
L'Avenue Office Tower Lt.21 Unit C, Jl. Raya Pasar Minggu Kav.16 Kel. Pancoran Kec. Pancoran , Jakarta Selatan
Registration Date
Oct 05, 2022
Expiry Date
Aug 01, 2024
Product Type
Serological Reagents
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STANDARD F TnI FIA
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STANDARD F iFOB FIA
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STANDARD F TnI/CK-MB Combo FIA
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STANDARD F NT-proBNP FIA
SD BIOSENSOR
STANDARD F CK-MB FIA
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STANDARD F D-dimer FIA
SD BIOSENSOR HEALTHCARE PVT. LTD.