ORTHO® 0.8% Red Cell Diluent - Indonesia BPOM Medical Device Registration
ORTHO® 0.8% Red Cell Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209022571. The device is manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is EMERALINDO ASIA PACIFIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ORTHO-CLINICAL DIAGNOSTICS, INC.Country of Origin
United States
Authorized Representative
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
Sep 13, 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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