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 21501420775. The device is manufactured by GE HEALTHCARE AUSTRIA GMBH & CO OG from Austria, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GE OPERATIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GE HEALTHCARE AUSTRIA GMBH & CO OGCountry of Origin
Austria
Authorized Representative
GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8
Registration Date
Nov 12, 2024
Expiry Date
Aug 01, 2028
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
Non Radiation Electromedics
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