M.I.ONE ENT Treatment Unit - Indonesia BPOM Medical Device Registration
M.I.ONE ENT Treatment Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10704120880. The device is manufactured by M.I.ONE CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
M.I.ONE CO., LTD.Country of Origin
Korea
Authorized Representative
PT. MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Mar 01, 2021
Expiry Date
Feb 24, 2025
Product Type
Therapeutic Ear, Nose and Throat Equipment
Ear, nose, and throat examination and treatment unit.
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