MGI High-throughput Automated Sample Preparation System - Indonesia BPOM Medical Device Registration
MGI High-throughput Automated Sample Preparation System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304320216. The device is manufactured by WUHAN MGI TECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is UBC MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WUHAN MGI TECH CO., LTD.Country of Origin
China
Authorized Representative
UBC MEDICAL INDONESIAAR Address
Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930
Registration Date
Sep 17, 2023
Expiry Date
May 31, 2026
Product Type
Immunology Laboratory Equipment and Reagents
RNA Preanalytical Systems.
Invitro Diagnostics
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
MGI Universal Sequencing Reaction Kit
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MGI Universal Sequencing Reaction Kit
WUHAN MGI TECH CO., LTD.
MGI Universal Sequencing Reaction Kit
WUHAN MGI TECH CO., LTD.
MGI Universal Sequencing Reaction Kit
WUHAN MGI TECH CO., LTD.