FUJIFILM Endoscopic CO2 Regulator - Indonesia BPOM Medical Device Registration
FUJIFILM Endoscopic CO2 Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801514892. The device is manufactured by FUJIFILM HEALTHCARE MANUFACTURING CORPORATION HANAMAKI 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
Mar 28, 2024
Expiry Date
Dec 31, 2027
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories.
Non Radiation Electromedics
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NITI - S Biliary Stent
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FUJIFILM Upper Gastrointestinal tract Scopes (Upper G.I. tract)
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FUJINON FUJIFILM Ultrasound Video Endoscope
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FUJIFILM Lower Gastrointestinal Tract Scopes (Lower G.I. Tract Scopes)
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