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MGI Universal Sequencing Reaction Kit - Indonesia BPOM Medical Device Registration

MGI Universal Sequencing Reaction Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204320644. The device is manufactured by WUHAN MGI TECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is UBC MEDICAL INDONESIA.

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 : A
MGI Universal Sequencing Reaction Kit
Analysis ID: AKL 10204320644

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

UBC MEDICAL INDONESIA

AR Address

Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930

Registration Date

Oct 31, 2023

Expiry Date

May 31, 2026

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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