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ONCOPROBE HBsAg Rapid Test - Indonesia BPOM Medical Device Registration

ONCOPROBE HBsAg Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305220029. The device is manufactured by FORMOSA BIOMEDICAL TECHNOLOGY CORP. from Taiwan (China), and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MAIN ONCOPROBE.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : D
ONCOPROBE HBsAg Rapid Test
Analysis ID: AKL 30305220029

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Taiwan (China)

Authorized Representative

PT. MAIN ONCOPROBE

AR Address

Apartemen Istana Harmoni Plaza Kompleks Harmoni Plaza, Jl. Suryopranoto 2 Unit 1M dan 2K, RT 2 RW 8 Desa/Kel. Gambir, Kec. Gambir, Kota AdmJakarta Pusat, Provinsi DKI Jakarta Kode Pos 10130

Registration Date

Feb 06, 2025

Expiry Date

Feb 04, 2028

Product Type

Immunological Test System

Antimitochondrial antibody immunological test system.

Invitro Diagnostics

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