FYSIOMED FISIOPHON 10800 - Indonesia BPOM Medical Device Registration
FYSIOMED FISIOPHON 10800 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403614556. The device is manufactured by FYSIOMED NV. from Belgium, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KIRANA JAYA LESTARI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FYSIOMED NV.Country of Origin
Belgium
Authorized Representative
PT. KIRANA JAYA LESTARIAR Address
JL. TANAH ABANG II NO. 37
Registration Date
Mar 07, 2020
Expiry Date
Aug 23, 2024
Product Type
Therapeutic Physical Health Equipment
Ultrasound and muscle stimulator for use in applying therapeutic deep heat for selected medical conditions
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