FUJIFILM Automatic X-RAY Developer Starter - Indonesia BPOM Medical Device Registration

FUJIFILM Automatic X-RAY Developer Starter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501710369. The device is manufactured by FUJIFILM ASIA PACIFIC PTE., LTD. from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FUJIFILM INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

FUJIFILM Automatic X-RAY Developer Starter

Analysis ID: AKL 21501710369

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

FUJIFILM ASIA PACIFIC PTE., LTD.

Country of Origin

Singapore

Authorized Representative

FUJIFILM INDONESIA

AR Address

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

Registration Date

Jul 02, 2021

Expiry Date

Jun 30, 2026

Product Type

Diagnostic Radiology Equipment

Automatic radiographic film processor.

Non Electromedic Non Sterile

DJ Fang

MedTech Regulatory Expert

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