FUJINON FUJIFILM Ultrasound Video Endoscope - Indonesia BPOM Medical Device Registration

FUJINON FUJIFILM Ultrasound Video Endoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801212980. 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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BPOM Registered

Risk Class Kelas Resiko : B

FUJINON FUJIFILM Ultrasound Video Endoscope

Analysis ID: AKL 20801212980

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

FUJIFILM CORPORATION CO., LTD

Country of Origin

Japan

Authorized Representative

PT. MEDISON JAYA RAYA

AR Address

JL. KAPT.P. TENDEAN NO.7, MAMPANG PRAPATAN

Registration Date

May 07, 2024

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Radiation Electromedics

DJ Fang

MedTech Regulatory Expert

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