ACUSON P500 Diagnostic Ultrasound System - Indonesia BPOM Medical Device Registration
ACUSON P500 Diagnostic Ultrasound System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321201. The device is manufactured by SIEMENS HEALTHCARE S.R.O from Slovakia, 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 HEALTHCARE S.R.OCountry of Origin
Slovakia
Authorized Representative
PT. SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88
Registration Date
Aug 17, 2023
Expiry Date
Jul 25, 2027
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
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