EUROPA All-In-One Solution - Indonesia BPOM Medical Device Registration
EUROPA All-In-One Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204812770. The device is manufactured by NEO VISION CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CREATIVE MANAGEMENT OPTICALS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NEO VISION CO., LTD.Country of Origin
Korea
Authorized Representative
PT. CREATIVE MANAGEMENT OPTICALSAR Address
Green Garden Blok A7/25 Jakarta Barat - 11520
Registration Date
Apr 19, 2021
Expiry Date
Apr 16, 2024
Product Type
Therapeutic Eye Equipment
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