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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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BPOM Registered
Risk Class Kelas Resiko : B
PROLINE Creatinine PAP FS
Analysis ID: AKL 20101324435

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. PRODIA MEDICAL DISTRIBUTION

AR 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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