GE Vivid iq - Indonesia BPOM Medical Device Registration
GE Vivid iq is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501711051. The device is manufactured by GE MEDICAL SYSTEMS (CHINA) C0., 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 SYSTEMS (CHINA) C0., 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
Sep 25, 2020
Expiry Date
Aug 29, 2024
Product Type
Diagnostic Radiology Equipment
Diagnostic ultrasonic transducer.
Non Radiation Electromedics
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