RUNMEI Saliva Collection Kit (Activated) - Indonesia BPOM Medical Device Registration
RUNMEI Saliva Collection Kit (Activated) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302127893. The device is manufactured by HUNAN RUNMEI GENE TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
HUNAN RUNMEI GENE TECHNOLOGY CO., LTDCountry of Origin
China
Authorized Representative
PT. FAITHFUL MEDICAL GRACEAR Address
Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89
Registration Date
Dec 13, 2021
Expiry Date
Jan 01, 2026
Product Type
Microbiology Equipment
Transport culture medium.
Invitro Diagnostics
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