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FUJI DRI-CHEM Slide NH3 - PII - Indonesia BPOM Medical Device Registration

FUJI DRI-CHEM Slide NH3 - PII is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101811597. The device is manufactured by FUJIFILM HEALTHCARE MANUFACTURING CORPORATION MINAMIASHIGARA NAKANUMA 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 Slide NH3 - PII
Analysis ID: AKL 20101811597

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 31, 2022

Expiry Date

Jun 24, 2025

Product Type

Clinical Chemistry Test System

Ammonia test system (card)

Invitro Diagnostics

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