FUJIFILM Processor Endoscope - Indonesia BPOM Medical Device Registration
FUJIFILM Processor Endoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801420400. 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 MEDISON JAYA RAYA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Japan
Authorized Representative
MEDISON JAYA RAYAAR Address
JL. KAPT.P. TENDEAN NO.7, MAMPANG PRAPATAN
Registration Date
Nov 18, 2024
Expiry Date
Dec 31, 2027
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories.
Non Radiation Electromedics
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