SOPHI System - Indonesia BPOM Medical Device Registration
SOPHI System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203220043. The device is manufactured by THIS AG from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is KHASANAH ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
THIS AGCountry of Origin
Switzerland
Authorized Representative
KHASANAH ALKESINDOAR Address
Jl. Prof. Dr. Soepomo SH, No.178A, Royal Palace B39, RT.001 RW.015, Menteng Dalam, Tebet
Registration Date
Jul 15, 2022
Expiry Date
Mar 02, 2025
Product Type
Surgical Eye Equipment
Phacofragmentation system.
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