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BIOREX Pregnancy Latex Tests - Indonesia BPOM Medical Device Registration

BIOREX Pregnancy Latex Tests is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421794. The device is manufactured by BIOREX DIAGNOSTICS LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SEGMED DISTRIBUTION 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.

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BPOM Registered
Risk Class Kelas Resiko : B
BIOREX Pregnancy Latex Tests
Analysis ID: AKL 20101421794

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

SEGMED DISTRIBUTION INDONESIA

AR Address

SEGMED DISTRIBUSI INDONESIA

Registration Date

Sep 12, 2024

Expiry Date

May 12, 2025

Product Type

Clinical Chemistry Test System

Human chorionic gonadotropin (HCG) test system

Invitro Diagnostics

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