FUJIFILM Diagnostic Ultrasound System - Indonesia BPOM Medical Device Registration
FUJIFILM Diagnostic Ultrasound System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501128010. The device is manufactured by FUJIFILM HEALTHCARE MANUFACTURING CORPORATION ANALYTICAL SYSTEMS KASHIWA FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FUJIFILM INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Japan
Authorized Representative
FUJIFILM INDONESIAAR Address
Eightyeight@Kasablanka Office Tower Lantai 36, Unit A, B dan C, Jl. Casablanca Kav. 88
Registration Date
Dec 17, 2021
Expiry Date
Jun 30, 2026
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
Non Radiation Electromedics
FUJIFILM Diagnostic Ultrasound System
FUJIFILM HEALTHCARE MANUFACTURING CORPORATION KASHIWA OFFICE
FUJIFILM Diagnostic Ultrasound System
FUJIFILM HEALTHCARE MANUFACTURING CORPORATION ANALYTICAL SYSTEM KASHIWA FACTORY
FUJIFILM Diagnostic Ultrasound System
FUJIFILM HEALTHCARE MANUFACTURING CORPORATION KASHIWA OFFICE
FUJIFILM Diagnostic Ultrasound System
FUJIFILM HEALTHCARE MANUFACTURING CORPORATION KASHIWA OFFICE
FUJIFILM Diagnostic Ultrasound System
FUJIFILM HEALTHCARE MANUFACTURING CORPORATION KASHIWA OFFICE
FUJIFILM Diagnostic Ultrasound System
UJIFILM HEALTHCARE MANUFACTURING CORPORATION KASHIWA OFFICE
FUJIFILM Diagnostic Ultrasound System
FUJIFILM HEALTHCARE MANUFACTURING CORPORATION KASHIWA OFFICE
FUJIFILM Diagnostic Ultrasound System
FUJIFILM HEALTHCARE MANUFACTURING CORPORATION KASHIWA OFFICE
FUJIFILM Diagnostic Ultrasound System
FUJIFILM HEALTHCARE MANUFACTURING CORPORATION KASHIWA OFFICE
FUJIFILM Diagnostic Ultrasound System
FUJIFILM HEALTHCARE MANUFACTURING CORPORATION KASHIWA OFFICE
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