HILAB WAS - Indonesia BPOM Medical Device Registration
HILAB WAS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421812. The device is manufactured by HI TECHNOLOGIES LTDA. from Brazil, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KIRANA JAYA LESTARI.
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HILAB Volt
Risk Classification
Product Class
Kelas : 2
Manufacturer
HI TECHNOLOGIES LTDA.Country of Origin
Brazil
Authorized Representative
PT. KIRANA JAYA LESTARIAR Address
Jl. Tanah Abang II No. 37 RT.001/RW.003, Kode Pos 10160, Kel. Petojo Selatan, Kec. Gambir, Kota Jakarta Pusat, Provinsi DKI Jakarta
Registration Date
Sep 17, 2024
Expiry Date
Jan 23, 2029
Product Type
Clinical Chemistry Test System
Multi parameter clinical chemistry test system
Invitro Diagnostics
HiLab Flow Ferritin
HiLab Flow PSA
HiLab Flow Cardiac Markers
HiLab Flow bHCG FIA
HiLab Flow HbA1c FIA
Hilab Volt AST
Hilab Flow
HILAB Volt ALT
HILAB Flow Dengue NS1
Hilab Lens CBC
HiLab Flow Ferritin
HI TECHNOLOGIES LTDA.
HiLab Flow bHCG FIA
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HILAB Volt ALT
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