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 10204520017. 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 DIASTIKA BIOTEKINDO.

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BPOM Registered

Risk Class Kelas Resiko : A

MGI Universal Sequencing Reaction Kit

Analysis ID: AKL 10204520017

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

WUHAN MGI TECH CO.,LTD

Country of Origin

China

Authorized Representative

DIASTIKA BIOTEKINDO

AR Address

Rukan Sentra Pemuda Kav.30 - 31 Jalan Pemuda No.61 RT.009 RW.003 Kel. Rawamangun Kec.Pulogadung

Registration Date

Jan 20, 2025

Expiry Date

Jun 10, 2027

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

DJ Fang

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MGI Universal Sequencing Reaction Kit

WUHAN MGI TECH CO.,LTD

MGI Universal Sequencing Reaction Kit - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

DJ Fang

MGI Universal Sequencing Reaction Kit

MGI Universal Sequencing Reaction Kit

MGI Universal Sequencing Reaction Kit

MGI Universal Sequencing Reaction Kit

MGI Universal Sequencing Reaction Kit

MGI Universal Sequencing Reaction Kit

MGI Universal Sequencing Reaction Kit

MGI Universal Sequencing Reaction Kit

MGI Universal Sequencing Reaction Kit

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MGI Universal Sequencing Reaction Kit

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