FUJIFILM Video Bronchoscope Therapeutic Type - Indonesia BPOM Medical Device Registration
FUJIFILM Video Bronchoscope Therapeutic Type is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20703420132. The device is manufactured by FUJIFILM HEALTHCARE MANUFACTURING CORPORATION SANO OFFICE 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
Country of Origin
Japan
Authorized Representative
PT. MEDISON JAYA RAYAAR Address
JL. KAPT.P. TENDEAN NO.7, MAMPANG PRAPATAN
Registration Date
Nov 23, 2024
Expiry Date
Dec 31, 2027
Product Type
Ear, Nose and Throat Surgical Equipment
Bronchoscope (flexible or rigid) and accessories.
Non Radiation Electromedics
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