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DSI Uric Acid FS TOOS - Indonesia BPOM Medical Device Registration

DSI Uric Acid FS TOOS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221794. The device is manufactured by DIASYS DIAGNOSTIC SYSTEM, GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDONESIAN SYSTEM DIAGNOSTICS.

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BPOM Registered
Risk Class Kelas Resiko : B
DSI Uric Acid FS TOOS
Analysis ID: AKL 20101221794

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. INDONESIAN SYSTEM DIAGNOSTICS

AR Address

Jl. Meruya Ilir Ruko Intercon Blok A-IX No 12B, Jakarta 11630

Registration Date

Apr 19, 2024

Expiry Date

Oct 20, 2025

Product Type

Clinical Chemistry Test System

Uric acid test system (kit & cair)

Invitro Diagnostics

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