SBL-3 Segmented Bifocal Lens - Indonesia BPOM Medical Device Registration
SBL-3 Segmented Bifocal Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202320103. The device is manufactured by LENSTEC (BARBADOS) INC. from Barbados, 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
Manufacturer
LENSTEC (BARBADOS) INC.Country of Origin
Barbados
Authorized Representative
YOTA MEDIKA INDONESIAAR Address
Ruko PulogadungTrade Center Blok 8-A No. 3 Lantai 1&2, Jl. Raya Bekasi KM 21
Registration Date
May 19, 2023
Expiry Date
Dec 31, 2026
Product Type
Prosthetic Eye Equipment
Intraocular lens.
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