PROLINE – b TruLab CRP hs Level 1 - Indonesia BPOM Medical Device Registration
PROLINE – b TruLab CRP hs Level 1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220236. The device is manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PRODIA DIAGNOSTIC LINE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIASYS DIAGNOSTIC SYSTEMS GMBHCountry of Origin
Germany
Authorized Representative
PRODIA DIAGNOSTIC LINEAR Address
Kawasan Industri Jababeka III Jl. Tekno 1 Blok C 2 D - E - F, Kel. Pasirgombong, Kec. Cikarang Utara, Kab. Bekasi, Jawa Barat Telp. 021-89872722
Registration Date
Mar 01, 2022
Expiry Date
Mar 01, 2025
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
Invitro Diagnostics

