DREAMLENS Bifocal Lens - Indonesia BPOM Medical Device Registration
DREAMLENS Bifocal Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204918013. 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 ILT INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SEE WORLD OPTICAL CO., LTDCountry of Origin
China
Authorized Representative
ILT INDONESIAAR Address
Ruko Mangga Dua Square Blok E No. 16, Jl. Gunung Sahari Raya No.1, Kel. Ancol, Kec. Pademangan, Jakarta Utara
Registration Date
Dec 06, 2019
Expiry Date
Jul 23, 2024
Product Type
Therapeutic Eye Equipment
Prescription show lens.
Non Electromedic Non Sterile
