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ALLPLEX™ GI-Parasite Assay - Indonesia BPOM Medical Device Registration

ALLPLEX™ GI-Parasite Assay is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303520056. The device is manufactured by SEEGENE INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SCIENCEWERKE.

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
ALLPLEX™ GI-Parasite Assay
Analysis ID: AKL 20303520056

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SEEGENE INC.

Country of Origin

Korea

Authorized Representative

PT. SCIENCEWERKE

AR Address

Jl.Palmerah Barat No.25

Registration Date

Jan 20, 2025

Expiry Date

Dec 31, 2026

Product Type

Serological Reagents

Gastrointestinal microorganism multiplex nucleic acid-based assay

Invitro Diagnostics

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DJ Fang

DJ Fang

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