THE UNFOLDER Platinum 1 Series Cartridge Implantation System - Indonesia BPOM Medical Device Registration
THE UNFOLDER Platinum 1 Series Cartridge Implantation System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203123296. The device is manufactured by AMO PUERTO RICO MANUFACTURING, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
AMO PUERTO RICO MANUFACTURING, INC.Country of Origin
United States
Authorized Representative
PT. BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Nov 20, 2024
Expiry Date
Aug 19, 2027
Product Type
Surgical Eye Equipment
Intraocular lens guide.
Non Electromedic Sterile
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