HYOTEK 1.8% Sodium Hyaluronate - Indonesia BPOM Medical Device Registration
HYOTEK 1.8% Sodium Hyaluronate is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203320474. The device is manufactured by TEKNOMEK MEDIKAL MALZEMELERI SANAYI VE TICARET LTDSTI. from Turkey, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is YOTA MEDIKA INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Country of Origin
Turkey
Authorized Representative
YOTA MEDIKA INDONESIAAR Address
Ruko PulogadungTrade Center Blok 8-A No. 3 Lantai 1&2, Jl. Raya Bekasi KM 21
Registration Date
Dec 19, 2023
Expiry Date
Nov 29, 2026
Product Type
Surgical Eye Equipment
Intraocular fluid.
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