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MAGLUMI ® H. pylori IgG (CLIA) - Indonesia BPOM Medical Device Registration

MAGLUMI ® H. pylori IgG (CLIA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220725. The device is manufactured by SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTIMEDILAB KARYAMANDIRI.

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BPOM Registered
Risk Class Kelas Resiko : B
MAGLUMI ® H. pylori IgG (CLIA)
Analysis ID: AKL 20303220725

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MULTIMEDILAB KARYAMANDIRI

AR Address

GP plaza lantai 3 unit 6, jalan Gelora II No. 01

Registration Date

Oct 24, 2022

Expiry Date

Dec 31, 2025

Product Type

Serological Reagents

Campylobacter fetus serological reagents.

Invitro Diagnostics

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