Multix Impact - Indonesia BPOM Medical Device Registration
Multix Impact is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220415. 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, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta
Registration Date
Jan 09, 2022
Expiry Date
Oct 12, 2023
Product Type
Diagnostic Radiology Equipment
Stationary x-ray system.
Electromedic Radiation
MULTIX Impact
SOMATOM go. Top
LUMINOUS Impulse
MULTIX Impact E
Somatom X.cite
Multix Impact C
Mammomat Select.
SOMATOM X.ceed
MULTIX Select DR X-ray System
SOMATOM go. Sim
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