THUASNE PediPro - Indonesia BPOM Medical Device Registration
THUASNE PediPro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903801788. 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
Registration Date
Dec 24, 2024
Expiry Date
Jan 07, 2026
Product Type
General Hospital Equipment and Other Individuals
Medical insole.
Non Electromedic Non Sterile
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