Luminous Fusion - Indonesia BPOM Medical Device Registration
Luminous Fusion is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501320831. The device is manufactured by SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.
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Luminos Fusion
Risk Classification
Product Class
Kelas : 2
Manufacturer
SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.Country of Origin
China
Authorized Representative
PT. SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl. Tahi Bonar Simatupang Kav. 88, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta
Registration Date
Mar 06, 2023
Expiry Date
Mar 31, 2025
Product Type
Diagnostic Radiology Equipment
Image-intensified fluoroscopic x-ray system.
Electromedic Radiation
MULTIX Impact
SOMATOM go. Top
LUMINOUS Impulse
MULTIX Impact E
Somatom X.cite
Multix Impact C
MULTIX Select DR X-ray System
SOMATOM X.ceed
Mammomat Select.
SOMATOM go. Sim
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