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DIALINE Magnesium - Indonesia BPOM Medical Device Registration

DIALINE Magnesium is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101026498. The device is manufactured by DIASYS DAIGNOSTIC SYSTEMS GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIATRON PROMEDIKA.

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
DIALINE Magnesium
Analysis ID: AKL 20101026498

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. DIATRON PROMEDIKA

AR Address

Perkantoran Plaza Pasifik Blok B2/41 Jl. Boulevard Barat Raya, Kelapa Gading

Registration Date

Feb 07, 2025

Expiry Date

Aug 01, 2029

Product Type

Clinical Chemistry Test System

Magnesium test system (kit & cair)

Invitro Diagnostics

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