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FUJI DRI-CHEM Mixing Cups - Indonesia BPOM Medical Device Registration

FUJI DRI-CHEM Mixing Cups is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203220104. The device is manufactured by FUJIFILM HEALTHCARE MANUFACTURING CORPORATION MINAMIASHIGARA NAKANUMA OFFICE from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is FUJIFILM INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
FUJI DRI-CHEM Mixing Cups
Analysis ID: AKL 10203220104

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Japan

Authorized Representative

FUJIFILM INDONESIA

AR Address

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

Registration Date

Sep 20, 2022

Expiry Date

Dec 06, 2024

Product Type

Pathology Equipment and Accessories

Specimen transport and storage container.

Invitro Diagnostics

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