Centricity RIS-i - Indonesia BPOM Medical Device Registration
Centricity RIS-i is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321078. The device is manufactured by GE HEALTHCARE from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is 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
Manufacturer
GE HEALTHCARECountry of Origin
United States
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
Jul 03, 2023
Expiry Date
May 04, 2026
Product Type
Diagnostic Radiology Equipment
Medical image management and processing system.
Non Radiation Electromedics
GE Centricity RIS-i
CENTRICITY Universal Viewer
CENTRICITY Universal Viewer Zero Footprint
CENTRICITY Enterprise Archive
GE Centricity PACS
Centricity Universal Viewer
CENTRICITY Radiology RA600
UNIVERSAL VIEWER
GE Enterprise Archive
GE Critical Care Suite
OEC One ASD
GE HUALUN MEDICAL SYSTEMS CO., LTD.
Vivid T8
GE MEDICAL SYSTEMS (CHINA) CO., LTD.
Vivid T9
GE MEDICAL SYSTEMS (CHINA) CO., LTD.
SIGNA Champion
GE HEALTHCARE (TIANJIN) COMPANY LIMITED
Voluson Expert 20
GE HEALTHCARE AUSTRIA GMBH & CO OG
Voluson Expert 22
GE HEALTHCARE AUSTRIA GMBH & CO OG
SIGNA Prime Elite
GE HEALTHCARE (TIANJIN) COMPANY LIMITED
ViewPoint 6
GE HEALTHCARE GMBH
LOGIQ E10
GE ULTRASOUND KOREA, LTD.
Voluson Signature 20
GE ULTRASOUND KOREA, LTD.

