NIKON VIDA 1.56 SP - Indonesia BPOM Medical Device Registration
NIKON VIDA 1.56 SP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204818754. The device is manufactured by SEE WORLD OPTICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. OPTICAL PARTNERS INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SEE WORLD OPTICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. OPTICAL PARTNERS INDONESIAAR Address
JL. TOMANG RAYA NO 15A, TOMANG GROGOL PETAMBURAN
Registration Date
Dec 14, 2018
Expiry Date
Dec 14, 2023
Product Type
Therapeutic Eye Equipment
Prescription show lens.
Non Electromedic Non Sterile
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