BECKMAN COULTER Access CEA Diluent - Indonesia BPOM Medical Device Registration
BECKMAN COULTER Access CEA Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306220043. The device is manufactured by BIO - RAD ,INC from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is DHH TRADING INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIO - RAD ,INCCountry of Origin
France
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
Jun 07, 2022
Expiry Date
Feb 10, 2026
Product Type
Tumor Antigen Immunologic Test System
Tumor-associated antigen immunological test system.
Invitro Diagnostics
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