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FUJI DRI-CHEM NX500i and Accessories - Indonesia BPOM Medical Device Registration

FUJI DRI-CHEM NX500i and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102710757. 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.

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BPOM Registered
Risk Class Kelas Resiko : B
FUJI DRI-CHEM NX500i and Accessories
Analysis ID: AKL 20102710757

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. FUJIFILM INDONESIA

AR Address

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

Registration Date

Oct 20, 2022

Expiry Date

Dec 06, 2024

Product Type

Clinical Laboratory Equipment

Enzyme analyzer for clinical use.

Invitro Diagnostics

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