ARTISAN Toric - Indonesia BPOM Medical Device Registration
ARTISAN Toric is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202710855. The device is manufactured by OPHTEC B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. KHASANAH ALKESINDO.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
OPHTEC B.V.Country of Origin
Netherlands
Authorized Representative
PT. KHASANAH ALKESINDOAR Address
Jl. Prof. Dr. Soepomo SH, No.178 A Royal Palace B 39. RT. 001 RW. 015, Prov. DKI Jakarta, Kota Jakarta Selatan, Kec. Tebet, Kel. Menteng Dalam
Registration Date
Jul 11, 2024
Expiry Date
Apr 04, 2027
Product Type
Prosthetic Eye Equipment
Intraocular lens.
Non Electromedic Sterile
ARTISAN Myopia
ARTISAN Aphakia
OPHTEC Enclavation Needle
ARTIFLEX Myopia
ARTIFLEX Toric
PRECIZON Monofocal
ARTIFLEX Insertion Spatula
PRECIZON Toric
PRECIZON Presbyopic
PRECIZON GO
OPHTEC B.V
FOCUS 8/0 PGA
AUROLAB
FOCUS 10/0 Nylon
AUROLAB
ARTISAN Myopia
OPHTEC B.V.
ARTISAN Aphakia
OPHTEC B.V.
OPHTEC Enclavation Needle
OPHTEC B.V.
ARTIFLEX Toric
OPHTEC B.V.
ARTIFLEX Myopia
OPHTEC B.V.
CATAGEL Plus Sodium Hyaluronate Ophthalmic Solution - 1.8%w/v
OPHTHALMIC TECHNOLOGY
CATAGEL Hydroxypropyl Methylcellulose Ophthalmic Solution-2%w/v
OPHTHALMIC TECHNOLOGY