Vivid T9 - Indonesia BPOM Medical Device Registration
Vivid T9 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420945. The device is manufactured by GE MEDICAL SYSTEMS (CHINA) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. 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 MEDICAL SYSTEMS (CHINA) CO., LTD.Country of Origin
China
Authorized Representative
GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8
Registration Date
Dec 22, 2024
Expiry Date
Sep 24, 2029
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
Non Radiation Electromedics
Vivid T8
VERSANA PREMIER Lotus ultrasound System
GE Invenia ABUS 2.0
Carestation 620 A1
Carestation 650c A1
Venue Go
Venue Fit
VERSANA ACTIVE
GE LOGIQ e
GE Logiq e
OEC One ASD
GE HUALUN MEDICAL SYSTEMS CO., LTD.
Vivid T8
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.
LOGIQ Fortis
GE ULTRASOUND KOREA, LTD.

