GE VIVID S70N - Indonesia BPOM Medical Device Registration
GE VIVID S70N is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220725. The device is manufactured by GE MEDICAL SYSTEM (CHINA), CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GE MEDICAL SYSTEM (CHINA), CO., LTD.Country of Origin
China
Authorized Representative
PT. GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lantai 18-19 Jl. R.A. Kartini, Kav. 8 Kel. Cilandak Barat, Kec. Cilandak Jakarta Selataran 12430
Registration Date
Jan 25, 2023
Expiry Date
Oct 17, 2027
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
Non Radiation Electromedics
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