THUASNE Pedipro Plus - Indonesia BPOM Medical Device Registration
THUASNE Pedipro Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903801789. 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
Oct 26, 2023
Expiry Date
Jan 07, 2026
Product Type
General Hospital Equipment and Other Individuals
Medical insole.
Non Electromedic Non Sterile
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