FUJIFILM Ultrasonic - Probe System - Indonesia BPOM Medical Device Registration
FUJIFILM Ultrasonic - Probe System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801123542. The device is manufactured by FUJIFILM CORPORATION CO.,LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDISON JAYA RAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FUJIFILM CORPORATION CO.,LTD.Country of Origin
Japan
Authorized Representative
PT. MEDISON JAYA RAYAAR Address
JL. KAPT.P. TENDEAN NO.7, MAMPANG PRAPATAN
Registration Date
Apr 25, 2024
Expiry Date
Dec 31, 2027
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories.
Non Radiation Electromedics
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