OXIFIVE Multi Purpose Solution - Indonesia BPOM Medical Device Registration
OXIFIVE Multi Purpose Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204806072. The device is manufactured by POLYTOUCH CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. OPTINDO SURYATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
POLYTOUCH CO., LTD.Country of Origin
Korea
Authorized Representative
PT. OPTINDO SURYATAMAAR Address
JL. IR H JUANDA III NO.10 B
Registration Date
Mar 06, 2020
Expiry Date
Jan 02, 2025
Product Type
Therapeutic Eye Equipment
Soft (hydrophilic) contact lens care products.
Non Electromedic Non Sterile
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POLYTOUCH CO., LTD.
HUNNY BUNNY Contact Lens
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POLYTOUCH CO., LTD.