FUJIFILM Sonosite Edge II Ultrasound System - Indonesia BPOM Medical Device Registration
FUJIFILM Sonosite Edge II Ultrasound System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501615750. The device is manufactured by FUJIFILM SONOSITE, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FUJIFILM INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FUJIFILM SONOSITE, INC.Country of Origin
United States
Authorized Representative
PT. FUJIFILM INDONESIAAR Address
Eightyeight@Kasablanka Office Tower Lantai 36, Unit A, B dan C, Jl. Casablanca Kav. 88
Registration Date
Jan 01, 2021
Expiry Date
Mar 31, 2025
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
Non Radiation Electromedics
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