PROLINE - b Magnesium XL FS - Indonesia BPOM Medical Device Registration
PROLINE - b Magnesium XL FS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101810809. The device is manufactured by DIASYS DIAGNOSTIC SYSTEM GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRODIA DIAGNOSTIC LINE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIASYS DIAGNOSTIC SYSTEM GMBH.Country of Origin
Germany
Authorized Representative
PT. 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
Dec 23, 2021
Expiry Date
Dec 23, 2024
Product Type
Clinical Chemistry Test System
Magnesium test system (kit & cair)
Invitro Diagnostics
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PROLINE โ a CRP U-hs
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PROLINE - b TruLab Cystatin C level 1
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PROLINE โ b TruCal CRP U
DIASYS DIAGNOSTIC SYSTEMS GMBH

