Mobius 3D - Indonesia BPOM Medical Device Registration
Mobius 3D is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21502220010. The device is manufactured by VARIAN MEDICAL SYSTEMS, INC. from United States, 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
VARIAN MEDICAL SYSTEMS, INC.Country of Origin
United States
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
Apr 24, 2022
Expiry Date
Jul 01, 2027
Product Type
Therapeutic Radiology Equipment
Medical charged-particle radiation therapy system.
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