PROTEOR Knee Knee Hytrek 1P130 - Indonesia BPOM Medical Device Registration
PROTEOR Knee Knee Hytrek 1P130 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402220172. The device is manufactured by PROTEOR from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ORTHOCARE INDONESIA.
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PROTEOR Genou Knee Hytrek 1P130
Risk Classification
Product Class
Kelas : 1
Manufacturer
PROTEORCountry of Origin
France
Authorized Representative
PT. ORTHOCARE INDONESIAAR Address
Ruko Galeri Niaga Mediterania 2 Blok N 8 J, Jalan Pantai Indah Utara II Rt/Rw : 007/008
Registration Date
Dec 12, 2024
Expiry Date
Mar 07, 2029
Product Type
Prosthetic Physical Health Equipment
External limb prosthetic component.
Non Electromedic Non Sterile
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