GE MaxFOV 2 - Indonesia BPOM Medical Device Registration
GE MaxFOV 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501127408. The device is manufactured by GEXPRO from United States, 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
GEXPROCountry of Origin
United States
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
Nov 29, 2021
Expiry Date
Sep 23, 2026
Product Type
Diagnostic Radiology Equipment
(Dihapus) Picture archiving and communications system.
Non Radiation Electromedics
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