TECNIS PureSee™ IOL with TECNIS Simplicity™ Delivery System - Indonesia BPOM Medical Device Registration
TECNIS PureSee™ IOL with TECNIS Simplicity™ Delivery System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202420015. The device is manufactured by AMO GRONINGEN B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
AMO GRONINGEN B.V.Country of Origin
Netherlands
Authorized Representative
BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Feb 19, 2024
Expiry Date
Aug 19, 2027
Product Type
Prosthetic Eye Equipment
Intraocular lens.
Non Electromedic Sterile
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