MULTIX Impact E - Indonesia BPOM Medical Device Registration
MULTIX Impact E is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501320991. 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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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
Registration Date
Jan 08, 2024
Expiry Date
Mar 09, 2028
Product Type
Diagnostic Radiology Equipment
Stationary x-ray system.
Electromedic Radiation
MULTIX Impact
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SOMATOM X.ceed
Mammomat Select.
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