FSV Pentax AS 1.60 Refine Inc - Indonesia BPOM Medical Device Registration
FSV Pentax AS 1.60 Refine Inc is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204420444. The device is manufactured by SHANGHAI CONANT OPTICS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. HOYA LENS INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SHANGHAI CONANT OPTICS CO., LTD.Country of Origin
China
Authorized Representative
PT. HOYA LENS INDONESIAAR Address
Wisma Lumbini , Lt3 , Jl Tomang Raya no:53 , Tomang ,Jakarta barat 11440
Registration Date
Sep 30, 2024
Expiry Date
Feb 10, 2028
Product Type
Therapeutic Eye Equipment
Prescription show lens.
Non Electromedic Non Sterile
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