Voluson Expert 20 - Indonesia BPOM Medical Device Registration
Voluson Expert 20 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220196. The device is manufactured by GE HEALTHCARE AUSTRIA GMBH AND CO OG from Austria, 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 HEALTHCARE AUSTRIA GMBH AND CO OGCountry of Origin
Austria
Authorized Representative
PT. GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8
Registration Date
Dec 17, 2024
Expiry Date
Aug 01, 2028
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
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