VIVID S60N - Indonesia BPOM Medical Device Registration
VIVID S60N is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501320754. The device is manufactured by GE VINGMED ULTRASOUND AS from Norway, 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 VINGMED ULTRASOUND ASCountry of Origin
Norway
Authorized Representative
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
Feb 01, 2023
Expiry Date
Oct 17, 2027
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
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