Voluson Expert 22 - Indonesia BPOM Medical Device Registration
Voluson Expert 22 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321484. The device is manufactured by GE HEALTHCARE AUSTRIA GMBH & CO OG from Austria, 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 HEALTHCARE AUSTRIA GMBH & CO OGCountry of Origin
Austria
Authorized Representative
GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lantai 18-19, JL. R.A. Kartini Kav. 8, Kelurahan Cilandak Barat, Kecamatan Cilandak, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, 12430
Registration Date
Dec 27, 2023
Expiry Date
Aug 01, 2028
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
Non Radiation Electromedics
VOLUSON Expert 18
Voluson Expert 20
Voluson Expert 22
GE Voluson E6
GE Voluson E10
GE Voluson E8
GE Voluson Expert 20
Voluson Expert 18
GE VOLUSON E10
Voluson E8
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.

