SD BIOSENSOR TB-Feron SPP - Indonesia BPOM Medical Device Registration
SD BIOSENSOR TB-Feron SPP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221381. The device is manufactured by SD BIOSENSOR from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. STANDARD BIOSENSOR INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SD BIOSENSORCountry of Origin
Korea
Authorized Representative
PT. STANDARD BIOSENSOR INDONESIAAR Address
L'AVENUE BUILDING UNIT C, LT. 21, JL. RAYA PASAR MINGGU KAV. 16
Registration Date
Aug 12, 2024
Expiry Date
Jan 18, 2029
Product Type
Clinical Chemistry Test System
Blood specimen collection device (kit & cair)
Invitro Diagnostics
STANDARD M10 DENV 1-4
STANDARD F TSH-II FIA
STANDARD Lipidocare Analyzer (NB)
STANDARD™ F hs-CRP
STANDARD F NT-proBNP FIA
STANDARD M10 MTB/NTM
STANDARD Q Dengue Duo Test
STANDARD™ Q H pylori Ab Test
STANDARD Q H pylori Ag Test
STANDARD H. pylori Ag Control
STANDARD M10 DENV 1-4
SD BIOSENSOR
STANDARD™ F Vitamin D FIA
SD BIOSENSOR HEALTHCARE PVT. LTD
STANDARD F TSH-II FIA
SD BIOSENSOR
STANDARD Lipidocare Analyzer (NB)
SD BIOSENSOR
VIASURE Zika, Dengue & Chikungunya Real Time PCR Detection Kit
CERTEST BIOTEC S.L
STANDARD™ Q HCV Ab Test
SD BIOSENSOR INC.
STANDARD F Dengue IgM/IgG FIA and Accessories
SD BIOSENSOR.
STANDARD™ F hs-CRP
SD BIOSENSOR
STANDARD F U-Albumin FIA amd Accessories
SD BIOSENSOR.
STANDARD M10 MTB/NTM
SD BIOSENSOR