PLATINUM Dengue Rapid Test Cassette (Whole Blood/Serum/Plasma) - Indonesia BPOM Medical Device Registration
PLATINUM Dengue Rapid Test Cassette (Whole Blood/Serum/Plasma) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420178. The device is manufactured by CITEST DIAGNOSTICS INC. from Canada, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PLATINUM MEDLAB INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CITEST DIAGNOSTICS INC.Country of Origin
Canada
Authorized Representative
PT. PLATINUM MEDLAB INDONESIAAR Address
Jl Raya Caman No.54 Jatibening Bekasi
Registration Date
May 07, 2024
Expiry Date
Dec 05, 2026
Product Type
Serological Reagents
Dengue virus serological reagents
Invitro Diagnostics
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