BECKMAN COULTER Access Sample Diluent A - Indonesia BPOM Medical Device Registration
BECKMAN COULTER Access Sample Diluent A is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204220112. The device is manufactured by BECKMAN COULTER INC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is DHH TRADING INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
BECKMAN COULTER INCCountry 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
May 17, 2022
Expiry Date
Feb 10, 2026
Product Type
Reagents and Specimen Providers
General purpose reagent.
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