SENO IRIS ™ - Indonesia BPOM Medical Device Registration
SENO IRIS ™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501520030. The device is manufactured by GE MEDICAL SYSTEMS SCS from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GE MEDICAL SYSTEMS SCSCountry of Origin
France
Authorized Representative
PT. GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8
Registration Date
Jan 17, 2025
Expiry Date
May 02, 2029
Product Type
Diagnostic Radiology Equipment
Medical image management and processing system.
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