STANDARD™ F hs-CRP - Indonesia BPOM Medical Device Registration
STANDARD™ F hs-CRP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305915525. 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
Sep 12, 2024
Expiry Date
Jan 18, 2029
Product Type
Immunological Test System
C-reactive protein immunological test system.
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