PROLINE Creatinine PAP FS - Indonesia BPOM Medical Device Registration
PROLINE Creatinine PAP FS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101324435. 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 GMBH.Country 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
Dec 05, 2023
Expiry Date
Dec 04, 2026
Product Type
Clinical Chemistry Test System
Creatine test system (kit & cair)
Invitro Diagnostics
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PROLINE TruCal ASO
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