Biograph Vision 450 Edge - Indonesia BPOM Medical Device Registration
Biograph Vision 450 Edge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501125591. The device is manufactured by SIEMENS MEDICAL SOLUTIONS USA., 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
SIEMENS MEDICAL SOLUTIONS USA., 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
Nov 08, 2022
Expiry Date
Aug 25, 2027
Product Type
Diagnostic Radiology Equipment
Emission computed tomography system.
Electromedic Radiation
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