OMNI Legend - Indonesia BPOM Medical Device Registration
OMNI Legend is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420910. The device is manufactured by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING from Israel, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGINGCountry of Origin
Israel
Authorized Representative
PT. GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8
Registration Date
Dec 17, 2024
Expiry Date
Jun 06, 2029
Product Type
Diagnostic Radiology Equipment
Emission computed tomography system.
Electromedic Radiation
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