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FUJI DRI-CHEM NX600 and Accessories - Indonesia BPOM Medical Device Registration

FUJI DRI-CHEM NX600 and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102126338. 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 FUJIFILM INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
FUJI DRI-CHEM NX600 and Accessories
Analysis ID: AKL 20102126338

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

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

Sep 20, 2024

Expiry Date

Feb 28, 2029

Product Type

Clinical Laboratory Equipment

Instrumentation for clinical multiplex test systems.

Invitro Diagnostics

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