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PROLINE Uric Acid FS TOOS - Indonesia BPOM Medical Device Registration

PROLINE Uric Acid FS TOOS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421422. 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 Uric Acid FS TOOS
Analysis ID: AKL 20101421422

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. PRODIA MEDICAL DISTRIBUTION

AR Address

Grha Prodia Utama Lantai 3 Unit 3 C, Jl. Raden Saleh No. 53

Registration Date

Jul 29, 2024

Expiry Date

Dec 21, 2028

Product Type

Clinical Chemistry Test System

Uric acid test system (kit & cair)

Invitro Diagnostics

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