FEMTIS Mplus Toric Intraocular Lens - Indonesia BPOM Medical Device Registration
FEMTIS Mplus Toric Intraocular Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202320171. The device is manufactured by TELEON SURGICAL B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is TRANSMEDIC INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
TELEON SURGICAL B.V.Country of Origin
Netherlands
Authorized Representative
TRANSMEDIC INDONESIAAR Address
PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137
Registration Date
Oct 04, 2023
Expiry Date
Dec 31, 2025
Product Type
Prosthetic Eye Equipment
Intraocular lens.
Non Electromedic Sterile
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