M.I.ONE LED Light Source - Indonesia BPOM Medical Device Registration
M.I.ONE LED Light Source is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801126946. The device is manufactured by M.I.ONE CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 2
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
Feb 02, 2022
Expiry Date
May 25, 2026
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories
Non Radiation Electromedics
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