SIGNA Voyager - Indonesia BPOM Medical Device Registration
SIGNA Voyager is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501320784. The device is manufactured by GE HEALTHCARE (TIANJIN) COMPANY LIMITED from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is GE OPERATIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GE HEALTHCARE (TIANJIN) COMPANY LIMITEDCountry of Origin
China
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
Feb 16, 2023
Expiry Date
Jul 23, 2025
Product Type
Diagnostic Radiology Equipment
Magnetic resonance diagnostic device.
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