ARTIFLEX Insertion Spatula - Indonesia BPOM Medical Device Registration
ARTIFLEX Insertion Spatula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203917959. The device is manufactured by OPHTEC B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. KHASANAH ALKESINDO.
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Risk Classification
Product Class
Kelas : 1
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. Kel. Menteng Dalam, Kec. Tebet, Jakarta Selatan.
Registration Date
Sep 02, 2023
Expiry Date
Apr 04, 2027
Product Type
Surgical Eye Equipment
Manual ophthalmic surgical instrument.
Non Electromedic Sterile
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.
ARTISAN Toric
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