FINECARE™ Dengue NS1 Ag Test - Indonesia BPOM Medical Device Registration
FINECARE™ Dengue NS1 Ag Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420652. The device is manufactured by GUANGZHOU WONDFO BIOTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CIPTA VARIA KHARISMA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGZHOU WONDFO BIOTECH CO., LTD.Country of Origin
China
Authorized Representative
PT. CIPTA VARIA KHARISMA UTAMAAR Address
Jl. Utan Kayu Raya No. 105A Jakarta
Registration Date
Dec 16, 2024
Expiry Date
May 22, 2029
Product Type
Serological Reagents
Dengue virus serological reagents
Invitro Diagnostics
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FINECARE™ FIA Meter II Plus SE
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FINECARE™ FSH Rapid Quantitative Test
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FINECARE™ AMH Rapid Quantitative Test
GUANGZHOU WONDFO BIOTECH CO., LTD.
FINECARE™ Estradiol (E2) Rapid Quantitative Test
GUANGZHOU WONDFO BIOTECH CO., LTD.
FINECARE™ Testosterone Rapid Quantitative Test
GUANGZHOU WONDFO BIOTECH CO., LTD.
FINECARE™ β-hCG Rapid Quantitative Test
GUANGZHOU WONDFO BIOTECH CO., LTD.
FINECARE™ Progesterone Rapid Quantitative Test
GUANGZHOU WONDFO BIOTECH CO., LTD.
FINECARE™ Prolactin Rapid Quantitative Test
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GUANGZHOU WONDFO BIOTECH CO., LTD.