GE Invenia ABUS Viewer - Indonesia BPOM Medical Device Registration
GE Invenia ABUS Viewer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501915247. 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 PT. 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
PT. GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lantai 18-19, JL. R.A. Kartini Kav. 8, Kelurahan Cilandak Barat, Kecamatan Cilandak, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, 12430
Registration Date
Dec 18, 2023
Expiry Date
Oct 19, 2027
Product Type
Diagnostic Radiology Equipment
(Dihapus) Picture archiving and communications system.
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