PROLINE TruCal RF - Indonesia BPOM Medical Device Registration
PROLINE TruCal RF is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101323999. 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
Oct 04, 2023
Expiry Date
Oct 01, 2026
Product Type
Clinical Chemistry Test System
Calibrator (cair)
Invitro Diagnostics
Proline TruLab L Level 2
PROLINE TruLab L Level 1
PROLINE TruCal U
PROLINE TruLab N
Yumizen C Urine Level 1 Control
PROLINE Uric Acid FS TOOS
DSI Urea FS
TruLab Urine Level 1
TruLab Urine Level 2
TRULAB Bicarbonate
Proline TruLab L Level 2
DIASYS DIAGNOSTIC SYSTEMS GMBH
PROLINE TruLab L Level 1
DIASYS DIAGNOSTIC SYSTEMS GMBH
PROLINE TruCal U
DIASYS DIAGNOSTIC SYSTEMS GMBH
PROLINE TruLab N
DIASYS DIAGNOSTIC SYSTEMS GMBH
PROLINE Uric Acid FS TOOS
DIASYS DIAGNOSTIC SYSTEMS GMBH
PROLINE Creatinine PAP FS
DIASYS DIAGNOSTIC SYSTEMS GMBH.
PROLINE TruCal ASO
DIASYS DIAGNOSTIC SYSTEMS GMBH
PROLINE Lactate FS
DIASYS DIAGNOSTIC SYSTEMS GMBH
PROLINE TruCal Protein
DIASYS DIAGNOSTIC SYSTEMS GMBH
PROLINE Bicarbonate FS
DIASYS DIAGNOSTIC SYSTEMS GMBH

