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DIASYSTEM Uric Acid (TBHBA) - Indonesia BPOM Medical Device Registration

DIASYSTEM Uric Acid (TBHBA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101324304. The device is manufactured by DIASYSTEM SCANDINAVIA AB from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DUAL NOBLE LIGHT.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
DIASYSTEM Uric Acid (TBHBA)
Analysis ID: AKL 20101324304

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Sweden

Authorized Representative

DUAL NOBLE LIGHT

AR Address

Ruko Villa Jatibening Toll Blok A no. 2 Jatibening - Bekasi

Registration Date

Nov 22, 2023

Expiry Date

May 25, 2027

Product Type

Clinical Chemistry Test System

Uric acid test system (kit & cair)

Invitro Diagnostics

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