FUJIFILM SYNAPSE VNA - Indonesia BPOM Medical Device Registration

FUJIFILM SYNAPSE VNA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501713671. The device is manufactured by FUJIFILM MEDICAL SYSTEM U.S.A., INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FUJIFILM INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

FUJIFILM SYNAPSE VNA

Analysis ID: AKL 21501713671

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

FUJIFILM MEDICAL SYSTEM U.S.A., INC.

Country of Origin

United States

Authorized Representative

PT. FUJIFILM INDONESIA

AR Address

Eightyeight@Kasablanka Office Tower Lantai 36, Unit A, B dan C, Jl. Casablanca Kav. 88

Registration Date

May 28, 2021

Expiry Date

May 27, 2026

Product Type

Diagnostic Radiology Equipment

(Dihapus) Picture archiving and communications system.

Non Radiation Electromedics

DJ Fang

MedTech Regulatory Expert

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Kelas Resiko : B