GE Invenia ABUS 2.0 - Indonesia BPOM Medical Device Registration
GE Invenia ABUS 2.0 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501913596. The device is manufactured by GE PARALLEL DESIGN, INC. 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 PARALLEL DESIGN, INC.Country of Origin
United States
Authorized Representative
PT. GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8
Registration Date
Dec 06, 2024
Expiry Date
Sep 11, 2029
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed echo imaging system.
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