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Oral/enteral medicine medicated administration kit, single-use

Access comprehensive regulatory information for Oral/enteral medicine medicated administration kit, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class Im is sponsored by Abbvie Pty Ltd, manufactured by Abbvie Inc in United States of America. The device registration started on March 02, 2021.

This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.

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TGA ARTG Official Data
Class Im
Class Im
Oral/enteral medicine medicated administration kit, single-use
Australia TGA ARTG Registered Device
Good Name: Abbvie Pty Ltd - Oral/enteral medicine medicated administration kit, single-use
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Intended Purpose

To ensure appropriate oral administration of the medicine component (Kaletra oral solution).

Device Classification
Risk Class
Class Im
Product Type
Procedure Pack
ARTG Category
General
Registration Information
Start Date
March 02, 2021
Effective Date
March 02, 2021
Sponsor
Manufacturer
Country
United States of America
Address
1 North Waukegan Road, North Chicago, IL, 60064