FRASER Clinical Centrifuge 4500 - Indonesia BPOM Medical Device Registration
FRASER Clinical Centrifuge 4500 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10205914498. The device is manufactured by DLAB SCIENTIFIC CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DIPA PUSPA LABSAINS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
DLAB SCIENTIFIC CO., LTD.Country of Origin
China
Authorized Representative
PT. DIPA PUSPA LABSAINSAR Address
Dipa Strategic Office, Lantai Lobby, Jl. Raya Kebayoran Lama No.28 RT.009/RW.011, Kel. Grogol Utara, Kec. Kebayoran Lama
Registration Date
Oct 22, 2021
Expiry Date
May 27, 2024
Product Type
Automatic and Semi-Automatic Hematology Equipment
Microsedimentation centrifuge.
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