MULTIX Fusion Max - Indonesia BPOM Medical Device Registration
MULTIX Fusion Max is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220364. The device is manufactured by SIEMENS HEALTHCARE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SIEMENS HEALTHCARE GMBH.Country of Origin
Germany
Authorized Representative
PT. SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88
Registration Date
Jun 16, 2023
Expiry Date
May 08, 2028
Product Type
Diagnostic Radiology Equipment
Stationary x-ray system.
Electromedic Radiation
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