Newtom GO 3D - Indonesia BPOM Medical Device Registration
Newtom GO 3D is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20601022164. The device is manufactured by CEFLA. S.C from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KIRANA JAYA LESTARI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CEFLA. S.CCountry of Origin
Italy
Authorized Representative
PT. KIRANA JAYA LESTARIAR Address
Jl. Tanah Abang II No. 37 RT.001/RW.003, Kode Pos 10160, Kel. Petojo Selatan, Kec. Gambir, Kota Jakarta Pusat, Provinsi DKI Jakarta
Registration Date
Sep 22, 2023
Expiry Date
Jun 08, 2028
Product Type
Diagnostic Dental Equipment
Extraoral source x-ray system.
Electromedic Radiation
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