O-SCAN - Indonesia BPOM Medical Device Registration
O-SCAN is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501026320. The device is manufactured by ESAOTE S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN MEDICAL SYNERGY.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ESAOTE S.P.A.Country of Origin
Italy
Authorized Representative
PT. MAIN MEDICAL SYNERGYAR Address
Komplek Taman Palem Lestari Blok P No. 3 Lantai 3
Registration Date
Oct 20, 2020
Expiry Date
Jul 01, 2025
Product Type
Diagnostic Radiology Equipment
Magnetic resonance diagnostic device.
Non Radiation Electromedics
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