PROTEUS XR/f - Indonesia BPOM Medical Device Registration
PROTEUS XR/f is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501913295. The device is manufactured by SOCIEDAD ESPAñOLA DE ELECTROMEDICINA Y CALIDAD (SEDECAL) S.A. from Spain, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Spain
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
Dec 19, 2023
Expiry Date
Nov 22, 2028
Product Type
Diagnostic Radiology Equipment
Stationary x-ray system.
Electromedic Radiation
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