Australia TGA ARTG recordVibratory intravascular recanalization system saline injector
Australia TGA ARTG Registered Device · Abbott Vascular Division of Abbott Medical Australia Pty Ltd · Cardiovascular Systems Inc · Class IIb · Started March 31, 2020
Good Name: Abbott Vascular Division of Abbott Medical Australia Pty Ltd - Vibratory intravascular recanalization system saline injector
- Risk Class
- Class IIb
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- March 31, 2020
- Effective Date
- March 31, 2020
- Country
- United States of America
- Address
- 1225 Old Highway 8 NW, Saint Paul, MN, 55112
The OAS pump provides the saline/lubricant pumping mechanism and power to the device. The small, reusable, and portable OAS pump attaches to a standard five wheel rolling intravenous (IV) pole and plugs in to a wall power outlet. The OAS pump includes a built-in, audible 25 second spin time notification, system power and priming buttons, and status indicators.
Access comprehensive regulatory information for Vibratory intravascular recanalization system saline injector in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Abbott Vascular Division of Abbott Medical Australia Pty Ltd, manufactured by Cardiovascular Systems Inc in United States of America. The device registration started on March 31, 2020.
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.