SIGNA Creator - Indonesia BPOM Medical Device Registration
SIGNA Creator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321283. The device is manufactured by GE HEALTHCARE MANUFACTURING LLC from United States, and is classified as Risk Class Kelas Resiko : C. 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
GE HEALTHCARE MANUFACTURING LLCCountry of Origin
United States
Authorized Representative
PT. 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
Nov 22, 2023
Expiry Date
Feb 23, 2028
Product Type
Diagnostic Radiology Equipment
Magnetic resonance diagnostic device.
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