ARTG 321544Medicine administration kit, percutaneous, medicated, single-use
ARTG ID: 321544 · Abbvie Pty Ltd · Abbvie Inc · Class I · Started August 09, 2019
Good Name: Abbvie Pty Ltd - Medicine administration kit, percutaneous, medicated, single-use
- Risk Class
- Class I
- Product Type
- Procedure Pack
- ARTG Category
- General
- ARTG ID
- 321544
- Start Date
- August 09, 2019
- Effective Date
- August 09, 2019
- Name
- Abbvie Pty Ltd
- Name
- Abbvie Inc
- Country
- United States of America
- Address
- 1 North Waukegan Road, North Chicago, IL, 60064
Skyrizi procedure pack containing a pre-filled syringe containing risankizumab solution for injection and a cleansing alcohol swab.
Access comprehensive regulatory information for Medicine administration kit, percutaneous, medicated, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 321544 and sponsored by Abbvie Pty Ltd, manufactured by Abbvie Inc in United States of America. The device registration started on August 09, 2019.
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.