iQ Precision Kit - Indonesia BPOM Medical Device Registration
iQ Precision Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101124118. The device is manufactured by BECKMAN COULTER INC. 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
BECKMAN COULTER INC.Country of Origin
United States
Authorized Representative
PT. DHH TRADING INDONESIAAR Address
Revenue Tower 19F, Jl. Jenderal Sudirman No. 52-53, Prov. DKI Jakarta, Kota Adm. Jakarta Selatan, Kec Kebayoran Baru, Kel Senayan
Registration Date
Dec 11, 2024
Expiry Date
Mar 28, 2029
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
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