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QIASTAT-DX Gastrointestinal Panel - Indonesia BPOM Medical Device Registration

QIASTAT-DX Gastrointestinal Panel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303917019. The device is manufactured by STAT-DX LIFE S.L. from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INODIA.

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
QIASTAT-DX Gastrointestinal Panel
Analysis ID: AKL 20303917019

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

STAT-DX LIFE S.L.

Country of Origin

Spain

Authorized Representative

PT. INODIA

AR Address

Perkantoran Kedoya Elok Plaza Blok DB no 24, Jalan Panjang, Kebon Jeruk

Registration Date

Oct 28, 2019

Expiry Date

Jul 12, 2024

Product Type

Serological Reagents

Gastrointestinal microorganism multiplex nucleic acid-based assay

Invitro Diagnostics

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