MGF 24/10 Genesi S - Indonesia BPOM Medical Device Registration
MGF 24/10 Genesi S is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10605915057. The device is manufactured by MGF S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. KIRANA JAYA LESTARI.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MGF S.R.L.Country 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
Jul 12, 2023
Expiry Date
May 19, 2028
Product Type
Other Dental Equipment
Dental operative unit and accessories.
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