REVOLUTION ACT - Indonesia BPOM Medical Device Registration
REVOLUTION ACT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501520026. The device is manufactured by WIPRO GE MEDICAL DEVICE MANUFACTURING PRIVATE LIMITED from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Country of Origin
India
Authorized Representative
PT. GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8
Registration Date
Jan 14, 2025
Expiry Date
Jul 17, 2029
Product Type
Diagnostic Radiology Equipment
Computed tomography x-ray system.
Electromedic Radiation
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LOGIQ E10
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