STANDARD F Dengue NS1 Ag FIA - Indonesia BPOM Medical Device Registration
STANDARD F Dengue NS1 Ag FIA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303816008. The device is manufactured by SD BIOSENSOR from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is STANDARD BIOSENSOR INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SD BIOSENSORCountry of Origin
Korea
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
Aug 26, 2022
Expiry Date
Dec 31, 2025
Product Type
Serological Reagents
Dengue virus serological reagents
Invitro Diagnostics
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