GE Definium XR120 - Indonesia BPOM Medical Device Registration
GE Definium XR120 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501918056. The device is manufactured by RAYENCE CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. 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
Manufacturer
RAYENCE CO., LTD.Country of Origin
Korea
Authorized Representative
PT. GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8
Registration Date
Jul 30, 2024
Expiry Date
May 16, 2029
Product Type
Diagnostic Radiology Equipment
Solid State X-Ray Imager (Flat Panel/Digital Imager)
Non Radiation Electromedics
VIVID S70N
GE VINGMED ULTRASOUND AS
SENO IRIS โข
GE MEDICAL SYSTEMS SCS
REVOLUTION ACT
WIPRO GE MEDICAL DEVICE MANUFACTURING PRIVATE LIMITED
Voluson Expert 22
GE HEALTHCARE AUSTRIA GMBH AND CO OG
GE Voluson Expert 18
GE HEALTHCARE AUSTRIA GMBH AND CO OG
LOGIQ E10
GE ULTRASOUND KOREA, LTD.
REVOLUTION Ascend Elite
GE HANGWEI MEDICAL SYSTEMS CO., LTD.
OMNI Legend
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
Voluson Expert 20
GE HEALTHCARE AUSTRIA GMBH AND CO OG
REVOLUTION Ascend Plus
GE HANGWEI MEDICAL SYSTEMS CO., LTD.

