GE LOGIQ P7 - Indonesia BPOM Medical Device Registration
GE LOGIQ P7 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501513391. The device is manufactured by GE ULTRASOUND KOREA LTD. from Korea, 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 ULTRASOUND KOREA LTD.Country of Origin
Korea
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
Mar 30, 2023
Expiry Date
Jan 04, 2026
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
Non Radiation Electromedics
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.

