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MGI Genetic Sequencer - Indonesia BPOM Medical Device Registration

MGI Genetic Sequencer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102420321. The device is manufactured by WUHAN MGI TECH CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DIASTIKA BIOTEKINDO.

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BPOM Registered
Risk Class Kelas Resiko : B
MGI Genetic Sequencer
Analysis ID: AKL 20102420321

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

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

Oct 07, 2024

Expiry Date

Jun 10, 2027

Product Type

Clinical Laboratory Equipment

High throughput genomic sequence analyzer for clinical use.

Invitro Diagnostics

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DJ Fang

DJ Fang

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