CITEST Malaria P.f./Pan Rapid Test Cassette (whole Blood) - Indonesia BPOM Medical Device Registration
CITEST Malaria P.f./Pan Rapid Test Cassette (whole Blood) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303320960. The device is manufactured by CITEST DIAGNOSTICS INC from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN MEDICAL CHAKRA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CITEST DIAGNOSTICS INCCountry of Origin
Canada
Authorized Representative
PT. MAIN MEDICAL CHAKRAAR Address
FORESTA BUSINESS LOFT 6 No. 10, Jl. Raya Boulevard Utara BSD City, Desa/Kelurahan Lengkong Kulon
Registration Date
Feb 09, 2023
Expiry Date
Jul 10, 2025
Product Type
Serological Reagents
Plasmodium species antigen detection assays
Invitro Diagnostics
CITEST™ Fluorescence Immunoassay Analyzer
CITEST ™ D-Dimer Test Cassette (Whole Blood/Plasma)
CITEST Multi-Drug 6 Drugs Rapid Test Panel (Urine) (MOP300/COC300/AMP1000/MET1000/THC50/BZO300)
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CITEST™ T3 Test Cassette (Serum/Plasma)
TSH Test Cassette (Serum/Plasma)
CITEST™ T4 Test Cassette (Serum/Plasma)
PLATINUM Influenza A+B Rapid Test Cassette (Swab/Nasal Aspirate)
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PLATINUM Dengue NS1 Rapid Test Cassette (Whole Blood/Serum/Plasma)
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