BECKMAN COULTER Access EPO - Indonesia BPOM Medical Device Registration
BECKMAN COULTER Access EPO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207220200. The device is manufactured by BECKMAN COULTER, INC (CHASKA) from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DHH TRADING INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BECKMAN COULTER, INC (CHASKA)Country of Origin
United States
Authorized Representative
DHH TRADING INDONESIAAR Address
Gedung World Trade Center 3, Lt. 20, Jl. Jend. Sudirman Kav. 29-31, Kel. Karet, Kec. Setiabudi, Jakarta Selatan, DKI Jakarta
Registration Date
Dec 26, 2022
Expiry Date
Feb 10, 2026
Product Type
Haematology Package and Kit
Erythropoietin assay.
Invitro Diagnostics
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