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XENTA D-Dimer Detection Kit (Fluorescent immune chromatography) - Indonesia BPOM Medical Device Registration

XENTA D-Dimer Detection Kit (Fluorescent immune chromatography) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305420267. The device is manufactured by XENTA BIOMEDICAL SCIENCE CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FOCUS DIAGNOSTIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
XENTA D-Dimer Detection Kit (Fluorescent immune chromatography)
Analysis ID: AKL 20305420267

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FOCUS 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

Jun 07, 2024

Expiry Date

Aug 02, 2028

Product Type

Immunological Test System

Multiparameter immunological test system

Invitro Diagnostics

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