AIM Rapid Test Dengue Tripleline-F - Indonesia BPOM Medical Device Registration
AIM Rapid Test Dengue Tripleline-F is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420589. The device is manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ACCURATE INTAN MADYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HANGZHOU ALLTEST BIOTECH CO., LTDCountry of Origin
China
Authorized Representative
PT. ACCURATE INTAN MADYAAR Address
KOMPLEK DUTA MERLIN, BLOK. F5 & F6, JL. GAJAH MADA NO. 3-5
Registration Date
Nov 09, 2024
Expiry Date
Nov 07, 2027
Product Type
Serological Reagents
Dengue virus serological reagents
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