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DxFLEX with Autoloader and Accessories - Indonesia BPOM Medical Device Registration

DxFLEX with Autoloader and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205918214. The device is manufactured by BECKMAN COULTER BIOTECHNOLOGY (SUZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FOKUS DIAGNOSTIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
DxFLEX with Autoloader and Accessories
Analysis ID: AKL 20205918214

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

FOKUS DIAGNOSTIC INDONESIA

AR Address

Jl. Jatipadang Raya No.9A, RT.6/RW.4, Kelurahan Jatipadang, Kecamatan Pasar Minggu, Kota Jakarta Selatan, DKI Jakarta 12540

Registration Date

Feb 10, 2025

Expiry Date

Dec 03, 2027

Product Type

Automatic and Semi-Automatic Hematology Equipment

Automated differential cell counter

Invitro Diagnostics

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