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 20102420307. 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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Risk Classification
Product Class
Kelas : 2
Manufacturer
WUHAN MGI TECH CO.,LTDCountry of Origin
China
Authorized Representative
DIASTIKA BIOTEKINDOAR Address
Rukan Sentra Pemuda Kav.30 - 31 Jalan Pemuda No.61 RT.009 RW.003 Kel. Rawamangun Kec.Pulogadung
Registration Date
Oct 01, 2024
Expiry Date
Jun 10, 2027
Product Type
Clinical Laboratory Equipment
High throughput genomic sequence analyzer for clinical use.
Invitro Diagnostics
MGI Universal Sequencing Reaction Kit
MGI Universal Sequencing Reaction Kit
MGI Universal Sequencing Reaction Kit
MGI Nucleic Acid Extraction Kit
MGI Universal Sequencing Reaction Kit
MGI DNA Sequencing Library Preparation System
MGI Genetic Sequencer DNBSEQ-G50
MGI Universal Sequencing Reaction Kit
MGI High-throughput Automated Sample Preparation System
MGI Universal Sequencing Reaction Kit
MGI Universal Sequencing Reaction Kit
WUHAN MGI TECH CO.,LTD
MGI Universal Sequencing Reaction Kit
WUHAN MGI TECH CO.,LTD
MGI DNA Sequencing Library Preparation System
WUHAN MGI TECH CO.,LTD
MGI Genetic Sequencer
WUHAN MGI TECH CO.,LTD
MGI Genetic Sequencer
WUHAN MGI TECH CO.,LTD
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