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iPro 2 Professional CGM System - Indonesia BPOM Medical Device Registration

iPro 2 Professional CGM System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101512498. The device is manufactured by MEDTRONIC MINIMED. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC 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 : C
iPro 2 Professional CGM System
Analysis ID: AKL 20101512498

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

MEDTRONIC MINIMED.

Country of Origin

United States

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Apr 17, 2020

Expiry Date

Mar 12, 2025

Product Type

Clinical Chemistry Test System

Glucose test system

Non Radiation Electromedics

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