BECKMAN COULTER CRP (Latex) Control Serum - Indonesia BPOM Medical Device Registration
BECKMAN COULTER CRP (Latex) Control Serum is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220606. The device is manufactured by CLINIQA CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DHH TRADING INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CLINIQA CORPORATIONCountry of Origin
United States
Authorized Representative
PT. 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 04, 2022
Expiry Date
Feb 10, 2026
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
Invitro Diagnostics
COBAS CRP Control cobas b 101
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