Dia Sure ® Dengue IgG/IgM Rapid Test Device (whole blood/serum/plasma) - Indonesia BPOM Medical Device Registration
Dia Sure ® Dengue IgG/IgM Rapid Test Device (whole blood/serum/plasma) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321181. The device is manufactured by ASSURE TECH. (HANGZOU) CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is VIPRO MEDITECH PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ASSURE TECH. (HANGZOU) CO., LTDCountry of Origin
China
Authorized Representative
VIPRO MEDITECH PRATAMAAR Address
Puri Metropolitan Blok G1/21, Petir
Registration Date
Jun 06, 2023
Expiry Date
Sep 20, 2027
Product Type
Serological Reagents
Dengue virus serological reagents
Invitro Diagnostics
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