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FUJINON FUJIFILM Upper Gastrointestinal Endoscope - Indonesia BPOM Medical Device Registration

FUJINON FUJIFILM Upper Gastrointestinal Endoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801714710. The device is manufactured by UJIFILM 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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BPOM Registered
Risk Class Kelas Resiko : B
FUJINON FUJIFILM Upper Gastrointestinal Endoscope
Analysis ID: AKL 20801714710

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. MEDISON JAYA RAYA

AR Address

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

Registration Date

Mar 26, 2024

Expiry Date

Dec 31, 2027

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Radiation Electromedics

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