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

FUJI DRI-CHEM Mixing Cups S is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203220085. 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 PT. FUJIFILM INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
FUJI DRI-CHEM Mixing Cups S
Analysis ID: AKL 10203220085

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

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

Aug 12, 2022

Expiry Date

Dec 16, 2024

Product Type

Pathology Equipment and Accessories

Specimen transport and storage container.

Invitro Diagnostics

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