ORTHO Vision Max Analyzer - Indonesia BPOM Medical Device Registration
ORTHO Vision Max Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209023370. The device is manufactured by TECAN SCHWEIZ AG from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. EMERALINDO ASIA PACIFIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TECAN SCHWEIZ AGCountry of Origin
Switzerland
Authorized Representative
PT. EMERALINDO ASIA PACIFICAR Address
Rukan Permata Senayan Blok G 15, Jl. Tentara Pelajar Rt/Rw 009/007, Kel. Grogol Utara Kec. Kebayoran Lama, Jakarta Selatan 12210
Registration Date
Nov 14, 2022
Expiry Date
Jun 21, 2024
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated blood grouping and antibody test system.
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