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UASURE Blood Uric Acid Monitoring System - Indonesia BPOM Medical Device Registration

UASURE Blood Uric Acid Monitoring System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101910675. The device is manufactured by APEX BIOTECHNOLOGY CORP. from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ISOTEKINDO INTERTAMA.

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BPOM Registered
Risk Class Kelas Resiko : B
UASURE Blood Uric Acid Monitoring System
Analysis ID: AKL 20101910675

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

ISOTEKINDO INTERTAMA

AR Address

Jl. Raya Kebayoran Lama No. 309 C Jakarta 12210

Registration Date

Sep 29, 2022

Expiry Date

Aug 14, 2027

Product Type

Clinical Chemistry Test System

Uric acid test system

Invitro Diagnostics

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