FUJIFILM Sonosite ST Ultrasound System - Indonesia BPOM Medical Device Registration
FUJIFILM Sonosite ST Ultrasound System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420606. 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 A, Lantai 36 Jl. Casablanca Raya Kav. 88, Desa/Kelurahan Menteng Dalam, Kec. Tebet, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12870 No Telp: 021-21282182
Registration Date
Sep 08, 2024
Expiry Date
Mar 31, 2026
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
Non Radiation Electromedics
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