THUASNE Ligaflex Pro - Indonesia BPOM Medical Device Registration
THUASNE Ligaflex Pro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402320578. The device is manufactured by THUASNE from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BETWEEN PARTNERS OF SELF-SUFFICIENCY.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
THUASNECountry of Origin
France
Authorized Representative
PT. BETWEEN PARTNERS OF SELF-SUFFICIENCYAR Address
Jl. Pos Pengumben Raya No.8 RT.005 RW.005, Sukabumi Selatan, Kebon Jeruk, Jakarta Barat 11560
Registration Date
Apr 02, 2023
Expiry Date
Nov 17, 2027
Product Type
Prosthetic Physical Health Equipment
Limb orthosis.
Non Electromedic Non Sterile
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