FISIOLINE Radiofrequency Instrument for Diathermy Therapy - Indonesia BPOM Medical Device Registration
FISIOLINE Radiofrequency Instrument for Diathermy Therapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421509. The device is manufactured by FISIOLINE S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HARLISA TRUE GRACE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FISIOLINE S.R.L.Country of Origin
Italy
Authorized Representative
PT. HARLISA TRUE GRACEAR Address
Jalan Sriti Blok HH-15, Perumahan Sedati Permai
Registration Date
Jul 11, 2024
Expiry Date
Feb 04, 2025
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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