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ABON HBsAg Hepatitis B Surface Antigen Rapid Test Device (Whole Blood/Serum/Plasma) - Indonesia BPOM Medical Device Registration

ABON HBsAg Hepatitis B Surface Antigen Rapid Test Device (Whole Blood/Serum/Plasma) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305024024. The device is manufactured by ABON BIOPHARM (HANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ALERE HEALTH.

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BPOM Registered
Risk Class Kelas Resiko : D
ABON HBsAg Hepatitis B Surface Antigen Rapid Test Device (Whole Blood/Serum/Plasma)
Analysis ID: AKL 30305024024

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

PT. ALERE HEALTH

AR Address

K-Link Tower Lantai 18 Zona D, E, dan F Jl. Gatot Subroto Kav. 59 A RT 001 RW 003 Kel. Kuningan Timur, Kec. Setiabudi, Jakarta Selatan

Registration Date

Oct 31, 2023

Expiry Date

Jun 04, 2027

Product Type

Immunological Test System

Antimitochondrial antibody immunological test system.

Invitro Diagnostics

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