Sensis Vibe Hemo - Indonesia BPOM Medical Device Registration
Sensis Vibe Hemo is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501126210. The device is manufactured by SIEMENS HEALTHINEERS AG from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SIEMENS HEALTHINEERS AGCountry of Origin
Germany
Authorized Representative
PT. SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88
Registration Date
Jul 29, 2024
Expiry Date
Mar 27, 2028
Product Type
Diagnostic Cardiology Equipment
Programmable diagnostic computer.
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