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XENTA TB Specific Cell Immune Response Detection kit - Indonesia BPOM Medical Device Registration

XENTA TB Specific Cell Immune Response Detection kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321040. The device is manufactured by XENTA BIOMEDICAL SCIENCE CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FOCUS DIAGNOSTIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
XENTA TB Specific Cell Immune Response Detection kit
Analysis ID: AKL 20303321040

Risk Classification

Kelas Resiko : C

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

Mar 22, 2023

Expiry Date

Sep 14, 2027

Product Type

Serological Reagents

Mycobacterium tuberculosis immunofluorescent reagents.

Invitro Diagnostics

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