Pure Global

ALINITY i HBsAg Reagent Kit - Indonesia BPOM Medical Device Registration

ALINITY i HBsAg Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305716004. The device is manufactured by ABBOTT IRELAND DIAGNOSTICS DIVISION. from Ireland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ABBOTT PRODUCTS INDONESIA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
ALINITY i HBsAg Reagent Kit
Analysis ID: AKL 20305716004

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Ireland

Authorized Representative

PT. ABBOTT PRODUCTS INDONESIA

AR Address

WISMA PONDOK INDAH 2 SUITE 1000, JL. SULTAN ISKANDAR MUDA KAV. V-TA

Registration Date

Oct 13, 2021

Expiry Date

Apr 20, 2026

Product Type

Immunological Test System

Antimitochondrial antibody immunological test system.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing