HELIANTHUS DBT - Indonesia BPOM Medical Device Registration
HELIANTHUS DBT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31501123654. The device is manufactured by METALTRONICA, S.P.A from Italy, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is GRATIA JAYA MULYA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
METALTRONICA, S.P.ACountry of Origin
Italy
Authorized Representative
GRATIA JAYA MULYAAR Address
Gading Park View, Jl. Boulevard Timur Raya Blok ZC I No. 10-11, RT.4/RW.11, Kel. Kelapa Gading Timur, Kec. Kelapa Gading, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta, Kode Pos 14250
Registration Date
Sep 21, 2023
Expiry Date
Dec 31, 2026
Product Type
Diagnostic Radiology Equipment
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Electromedic Radiation
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