OPTACT Revision Overnight Wear Orthokeratology Contact Lens - Indonesia BPOM Medical Device Registration
OPTACT Revision Overnight Wear Orthokeratology Contact Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204220506. The device is manufactured by VISION TECHNOLOGY CO., LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CEKINDO BUSINESS INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VISION TECHNOLOGY CO., LTD.Country of Origin
Taiwan (China)
Authorized Representative
PT. CEKINDO BUSINESS INTERNATIONALAR Address
CEKINDO BUSINESS INTERNATIONAL
Registration Date
Dec 23, 2022
Expiry Date
Nov 29, 2027
Product Type
Therapeutic Eye Equipment
Overnight contact lens orthokeratology
Non Electromedic Non Sterile
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