Venue Fit - Indonesia BPOM Medical Device Registration
Venue Fit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501320904. The device is manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES - CRITIKON DE MEXICO S. DE R.L. DE C.V. from Mexico, 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
Country of Origin
Mexico
Authorized Representative
PT. GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8
Registration Date
Jun 22, 2024
Expiry Date
Oct 19, 2027
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
Non Radiation Electromedics
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