ARIA Malaria Pf/Pan Ag Rapid Test - Indonesia BPOM Medical Device Registration

ARIA Malaria Pf/Pan Ag Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321144. The device is manufactured by BEIJING GENESEE BIOTECH, INC from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HERMAN MEDTEK DIAGNOSTICS.

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BPOM Registered

Risk Class Kelas Resiko : B

ARIA Malaria Pf/Pan Ag Rapid Test

Analysis ID: AKL 20303321144

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

BEIJING GENESEE BIOTECH, INC

Country of Origin

China

Authorized Representative

PT. HERMAN MEDTEK DIAGNOSTICS

AR Address

Jl. Lingkar Luar Barat, Puri Kembangan, Komplek Rukan Puri Mansion Blok A No.16 Kel.Kembangan Selatan Kec.Kembangan, Kota Jakarta Barat, DKI Jakarta

Registration Date

May 20, 2023

Expiry Date

Jun 04, 2025

Product Type

Serological Reagents

Plasmodium species antigen detection assays

Invitro Diagnostics

DJ Fang

MedTech Regulatory Expert

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Products from the same manufacturer (6 products)

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ARIA PSA Semi-Quantitative Rapid Test

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Kelas Resiko : A

ELECTROLINE 100 Reference Electrode Filling Solution

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Kelas Resiko : C

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Electroline 100 pH Na Cl Electrode Filling Solution

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Kelas Resiko : C

MDX Hemaline 500 Staining Solution

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Kelas Resiko : A

HEMALINE 500 Diluent

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