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QIAGEN Rotor-Gene Q MDx 5Plex and accessories - Indonesia BPOM Medical Device Registration

QIAGEN Rotor-Gene Q MDx 5Plex and accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304122816. The device is manufactured by PLEXUS MANUFACTURING SDN BHD from Malaysia, and is classified as Risk Class Kelas Resiko : C. 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 : C
QIAGEN Rotor-Gene Q MDx 5Plex and accessories
Analysis ID: AKL 20304122816

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

PT. INODIA

AR Address

Jalan Panjang, Perkantoran Kedoya Elok Plaza Blok DB No. 24

Registration Date

Jun 06, 2023

Expiry Date

Dec 10, 2025

Product Type

Immunology Laboratory Equipment and Reagents

RNA Preanalytical Systems.

Invitro Diagnostics

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