GE Critical Care Suite - Indonesia BPOM Medical Device Registration
GE Critical Care Suite is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501123227. The device is manufactured by GE HEALTHCARE 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
GE HEALTHCARECountry 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
Jun 02, 2021
Expiry Date
Aug 03, 2025
Product Type
Diagnostic Radiology Equipment
(Dihapus) Picture archiving and communications system.
Non Radiation Electromedics
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