Each one is a foot - Indonesia BPOM Medical Device Registration
Each one is a foot is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402420078. The device is manufactured by PROTEOR from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is ORTHOCARE INDONESIA.
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PROTEOR Exalto Foot
Risk Classification
Product Class
Kelas : 1
Manufacturer
PROTEORCountry of Origin
France
Authorized Representative
ORTHOCARE INDONESIAAR Address
Ruko Galeri Niaga Mediterania 2 Blok N 8 J, Jalan Pantai Indah Utara II Rt/Rw : 007/008
Registration Date
Dec 13, 2024
Expiry Date
Mar 07, 2029
Product Type
Prosthetic Physical Health Equipment
Prosthetic and orthotic accessory.
Non Electromedic Non Sterile
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