MAGNETOM Free.Max - Indonesia BPOM Medical Device Registration
MAGNETOM Free.Max is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501125391. The device is manufactured by SIEMENS HEALTHCARE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SIEMENS HEALTHCARE GMBH.Country of Origin
Germany
Authorized Representative
PT. SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl. Tahi Bonar Simatupang Kav. 88, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta
Registration Date
Sep 01, 2021
Expiry Date
Dec 06, 2024
Product Type
Diagnostic Radiology Equipment
Magnetic resonance diagnostic device.
Non Radiation Electromedics
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