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 21501420510. The device is manufactured by GE HUALUN MEDICAL SYSTEMS CO., LTD. from China, 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 HUALUN MEDICAL SYSTEMS CO., LTD.Country of Origin
China
Authorized Representative
PT. GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8
Registration Date
Aug 08, 2024
Expiry Date
Sep 25, 2028
Product Type
Diagnostic Radiology Equipment
Emission computed tomography system.
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