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FUJIFILM FDR D-EVO GL - Indonesia BPOM Medical Device Registration

FUJIFILM FDR D-EVO GL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501817504. The device is manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FUJIFILM INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
FUJIFILM FDR D-EVO GL
Analysis ID: AKL 21501817504

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. FUJIFILM INDONESIA

AR Address

: EightyEight@Kasablanka Office Tower A, Lantai 36 Jl. Casablanca Raya Kav. 88, Desa/Kelurahan Menteng Dalam, Kec. Tebet, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12870 No Telp: 021-21282182

Registration Date

Jan 17, 2025

Expiry Date

Jun 30, 2029

Product Type

Diagnostic Radiology Equipment

Medical image digitizer.

Non Radiation Electromedics

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