Vivid iq - Indonesia BPOM Medical Device Registration
Vivid iq is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501320868. The device is manufactured by GE MEDICAL SYSTEMS (CHINA) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GE OPERATIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GE MEDICAL SYSTEMS (CHINA) CO., LTD.Country of Origin
China
Authorized Representative
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
Mar 29, 2023
Expiry Date
Jan 24, 2027
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
Non Radiation Electromedics
Vivid iq
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Vivid iq
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Vivid iq
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Vivid iq
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