PROLINE Bicarbonate FS - Indonesia BPOM Medical Device Registration
PROLINE Bicarbonate FS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101323755. 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 PT. PRODIA MEDICAL DISTRIBUTION.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIASYS DIAGNOSTIC SYSTEMS GMBHCountry of Origin
Germany
Authorized Representative
PT. PRODIA MEDICAL DISTRIBUTIONAR Address
Kawasan Industri Jababeka III, Jalan Tekno 1 Blok C 2 D Lantai 1 Lot 1
Registration Date
Aug 30, 2023
Expiry Date
Aug 29, 2026
Product Type
Clinical Chemistry Test System
Bicarbonate/carbon dioxide test system (kit & cair)
Invitro Diagnostics
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