LUMINOUS Impulse - Indonesia BPOM Medical Device Registration
LUMINOUS Impulse is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220699. 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 SIEMENS HEALTHINEERS INDONESIA.
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LUMINOS Impulse
Risk Classification
Product Class
Kelas : 2
Manufacturer
SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.Country of Origin
China
Authorized Representative
SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88
Registration Date
Nov 15, 2024
Expiry Date
May 08, 2028
Product Type
Diagnostic Radiology Equipment
Image-intensified fluoroscopic x-ray system.
Electromedic Radiation
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